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Belotero Balance is a hyaluronic-acid based dermal filler approved for injection into the mid-to-deep dermis for correction of moderate-to-severe facial wrinkles and folds, such as nasolabial folds. The device is a kitted pack containing: (1) a pre-filled, sterile Belotero Balance gel in a 1 mL syringe, (2) two sterile needles (27G x 1/2 in, 30G x 1/2 in), and (3) two patient record labels.
ANTEIS SA
8700M0
In Commercial Distribution
- 07640123791121 ()
- Total Volume: 1 Milliliter
- Needle Gauge: 27 Gauge
- Needle Gauge: 30 Gauge
- Dermal tissue reconstructive material, microbe-derived
The surgical drainage is a sterile and single-use device. Flat low profile helps promote tissue plane approximation. The drainage has depth markings, graduated from the end of the perforated section: these markings facilitate accurate positioning of the drainage in the wound. The drainage is biocompatible and hemocompatible (in accordance with the regulations in force). The product is compatible for use with gravity or suction drainage systems.
REDAX SPA
24141
In Commercial Distribution
- 18034139294596 ()
- 08034139294599 ()
24141
- Closed-wound drain, non-bioabsorbable
The surgical drainage is a sterile and single-use device. Flat low profile helps promote tissue plane approximation. The drainage has depth markings, graduated from the end of the perforated section: these markings facilitate accurate positioning of the drainage in the wound. The drainage is biocompatible and hemocompatible (in accordance with the regulations in force). The product is compatible for use with gravity or suction drainage systems.
REDAX SPA
24140
In Commercial Distribution
- 18034139294589 ()
- 08034139294582 ()
24140
- Closed-wound drain, non-bioabsorbable
The surgical drainage is a sterile and single-use device. Flat low profile helps promote tissue plane approximation. The drainage has depth markings, graduated from the end of the perforated section: these markings facilitate accurate positioning of the drainage in the wound. The drainage is biocompatible and hemocompatible (in accordance with the regulations in force). The product is compatible for use with gravity or suction drainage systems.
REDAX SPA
24131
In Commercial Distribution
- 18034139294572 ()
- 08034139294575 ()
24131
- Closed-wound drain, non-bioabsorbable
The surgical drainage is a sterile and single-use device. Flat low profile helps promote tissue plane approximation. The drainage has depth markings, graduated from the end of the perforated section: these markings facilitate accurate positioning of the drainage in the wound. The drainage is biocompatible and hemocompatible (in accordance with the regulations in force). The product is compatible for use with gravity or suction drainage systems.
REDAX SPA
24130
In Commercial Distribution
- 18034139294565 ()
- 08034139294568 ()
24130
- Closed-wound drain, non-bioabsorbable
The surgical drainage is a sterile and single-use device. Flat low profile helps promote tissue plane approximation. The drainage has depth markings, graduated from the end of the perforated section: these markings facilitate accurate positioning of the drainage in the wound. The drainage is biocompatible and hemocompatible (in accordance with the regulations in force). The product is compatible for use with gravity or suction drainage systems.
REDAX SPA
24111
In Commercial Distribution
- 18034139294534 ()
- 08034139294537 ()
24111
- Closed-wound drain, non-bioabsorbable
The surgical drainage is a sterile and single-use device. Flat low profile helps promote tissue plane approximation. The drainage has depth markings, graduated from the end of the perforated section: these markings facilitate accurate positioning of the drainage in the wound. The drainage is biocompatible and hemocompatible (in accordance with the regulations in force). The product is compatible for use with gravity or suction drainage systems.
REDAX SPA
24110
In Commercial Distribution
- 18034139294527 ()
- 08034139294520 ()
24110
- Closed-wound drain, non-bioabsorbable
HYMOVIS® is based on an ultra-pure hyaluronan engineered using a proprietary process to increase viscosity, elasticity and residence time without chemical crosslinking.The hyaluronan in HYMOVIS® is derived from bacterial fermentation. HYMOVIS® is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy or simple analgesics (e.g., acetaminophen).
FIDIA FARMACEUTICI SPA
FID185704
Not in Commercial Distribution
- M71389122496630SAM1 ()
- M71389122496630SAM0 ()
- Total Volume: 3 Milliliter
FID185704
- Synovial fluid supplementation medium
HYMOVIS® is based on an ultra-pure hyaluronan engineered using a proprietary process to increase viscosity, elasticity and residence time without chemical crosslinking.The hyaluronan in HYMOVIS® is derived from bacterial fermentation. HYMOVIS® is indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy or simple analgesics (e.g., acetaminophen).
FIDIA FARMACEUTICI SPA
89122-4966-30
Not in Commercial Distribution
- M71389122496630A16 ()
- M71389122496630A ()
- Total Volume: 3 Milliliter
89122-4966-30
- Synovial fluid supplementation medium
CardioCel® 3D is prepared from bovine pericardium using the ADAPT® Tissue Processing Technology.
The pericardium is procured from cattle originating in Australia. Australia is considered as being of negligible risk
for BSE.
The device is a sterile, off-white, moist, pre-cut, flat or curved sheet of acellular collagen, presented sterile in a
solution of propylene glycol and sealed in a container impermeable to air and moisture.
ADMEDUS REGEN PTY LTD
UC0307A90
In Commercial Distribution
- 09348992000327 ()
- Width: 3 Centimeter
- Length: 7 Centimeter
- Angle: 90 degree
C0307A90
- Cardiovascular patch, animal-derived