SEARCH RESULTS FOR: 仿制圣彼得堡国立交通大学毕业证{官网:ｚｊｗ２１１.ｃｏｍ}株洲得克萨斯A(72107 results)
Only the first 10,000 results were returned. Filter these results or refine your query. Some pre-built queries with more than 10,000 results are available for download.
FLAIR® Endovascular Stent Graft 7 mm x 30 mm (80 cm delivery catheter)(flared)
Bard Peripheral Vascular, Inc.
FAF07030
Not in Commercial Distribution
- 04049519008776 ()
- 14049519008773 ()
- Implant Diameter,7 Millimeter
- Catheter Length,80 Centimeter
- Implant Length,30 Millimeter
FAF07030
- Peripheral artery endovascular stent-graft, non-medicated
FLAIR® Endovascular Stent Graft 6 mm x 70 mm (80 cm delivery catheter)(flared)
Bard Peripheral Vascular, Inc.
FAF06070
Not in Commercial Distribution
- 04049519008769 ()
- 14049519008766 ()
- Catheter Length,80 Centimeter
- Implant Length,70 Millimeter
- Implant Diameter,6 Millimeter
FAF06070
- Peripheral artery endovascular stent-graft, non-medicated
FLAIR® Endovascular Stent Graft 6 mm x 50 mm (80 cm delivery catheter)(flared)
Bard Peripheral Vascular, Inc.
FAF06050
Not in Commercial Distribution
- 04049519008752 ()
- 14049519008759 ()
- Implant Length,50 Millimeter
- Catheter Length,80 Centimeter
- Implant Diameter,6 Millimeter
FAF06050
- Peripheral artery endovascular stent-graft, non-medicated
FLAIR® Endovascular Stent Graft 6 mm x 40 mm (80 cm delivery catheter)(flared)
Bard Peripheral Vascular, Inc.
FAF06040
Not in Commercial Distribution
- 04049519008745 ()
- 14049519008742 ()
- Catheter Length,80 Centimeter
- Implant Diameter,6 Millimeter
- Implant Length,40 Millimeter
FAF06040
- Peripheral artery endovascular stent-graft, non-medicated
FLAIR® Endovascular Stent Graft 6 mm x 30 mm (80 cm delivery catheter)(flared)
Bard Peripheral Vascular, Inc.
FAF06030
Not in Commercial Distribution
- 04049519008738 ()
- 14049519008735 ()
- Catheter Length,80 Centimeter
- Implant Diameter,6 Millimeter
- Implant Length,30 Millimeter
FAF06030
- Peripheral artery endovascular stent-graft, non-medicated
The BreathTek UBT for H. pylori Kit (BreathTek UBT Kit) is intended for use in the qualitative detection of urease associated with H. pylori in the human stomach and is indicated as an aid in the initial diagnosis and post-treatment monitoring of H. pylori infection in adults, and pediatric patients 3 to 17 years old. The test may be used for monitoring treatment is used at least 4 weeks following completion of therapy. For there purposes, the system utilizes an Infrared Spectrophotometer for the measurement of the ration of 13CO2 to 12CO2 in breath samples, in clinical laboratories and point-of-care settings. The Pediatric Urea Hydrolysis Rate Calculation Application (pUHR-CA), provided as a web-based calculation program, is required to obtain pediatric test results. The BreathTek UBT Kit is for administration by the heath care professional, as ordered by a licensed health care practitioner.
MERIDIAN BIOSCIENCE, INC.
01
In Commercial Distribution
- 00840733101434 ()
- 00840733101441 ()
8209
- Helicobacter pylori urease IVD, kit, chromogenic
Radiesse Injectable Implant is a volumizing filler indicated for subdermal implantation for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds and it is also intended for restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus. Radiesse Volumizing Filler Kit contains (1) injectable implant and (2) 27 gauge thin walled x 0.75 inch needles.
MERZ NORTH AMERICA, INC.
8071M0K1
In Commercial Distribution
- M2138071M0K15 ()
- Total Volume: 1.5 Milliliter
- Dermal tissue reconstructive material, synthetic mineral
Radiesse Injectable Implant is a volumizing filler indicated for subdermal implantation for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds and it is also intended for restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus. Radiesse Volumizing Filler Kit contains (1) injectable implant and (2) 27 gauge thin walled x 0.75 inch needles.
MERZ NORTH AMERICA, INC.
8069M0K1
In Commercial Distribution
- M2138069M0K15 ()
- Total Volume: 0.8 Milliliter
- Dermal tissue reconstructive material, synthetic mineral
The TherOx DownStream System, is indicated for the preparation and delivery of SuperSaturated Oxygen Therapy (SSO2 Therapy) to targeted ischemic regions perfused
by the patient’s left anterior descending coronary artery immediately following revascularization by means of percutaneous coronary intervention (PCI) with stenting
that has been completed within 6 hours after the onset of anterior acute myocardial infarction (AMI) symptoms caused by a left anterior descending artery infarct lesion.
THEROX, INC.
SSO2 - 5.0
In Commercial Distribution
- 20862478000463 ()
- 00862478000469 ()
- 10862478000466 ()
- 5F
- Supersaturated oxygen therapy system catheter
The TherOx DownStream System, is indicated for the preparation and delivery of SuperSaturated Oxygen Therapy (SSO2 Therapy) to targeted ischemic regions perfused
by the patient’s left anterior descending coronary artery immediately following revascularization by means of percutaneous coronary intervention (PCI) with stenting
that has been completed within 6 hours after the onset of anterior acute myocardial infarction (AMI) symptoms caused by a left anterior descending artery infarct lesion.
THEROX, INC.
SSO2 - 4.5
In Commercial Distribution
- 20862478000456 ()
- 00862478000452 ()
- 10862478000459 ()
- 5F
- Supersaturated oxygen therapy system catheter