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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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ML7040 (Minus 20) - 00850724001049

Sterile Disposable microkeratome blade, for use on the Alcon SKBM Microkeratome
MED LOGICS INC
ML7040 (-20)
In Commercial Distribution

  • 10850724001046 ()
  • 00850724001049 ()
ML7040 (-20)

  • Keratome blade, single-use

Triever 20 Curve - 00850291007215

Triever 20 Catheter, 20 Fr, 105 cm
INARI MEDICAL INC
21-201
In Commercial Distribution

  • 00850291007215 ()

  • Outer Diameter: 6.5 Millimeter
  • Catheter Working Length: 105 Centimeter


  • Thrombectomy suction catheter

Diver 20° Right - 10810190017910

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution

  • 10810190017910 ()
748211

  • Cast cutting shears

Grasper 20° Left - 10810190017132

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution

  • 10810190017132 ()
391421t

  • Clamp manipulation forceps

Grasper 20° Right - 10810190017125

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution

  • 10810190017125 ()
391411t

  • Clamp manipulation forceps

Hip Curette, 20° - 10810190015916

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
E
In Commercial Distribution

  • 10810190015916 ()
904441st

  • Bone curette, reusable

Diver 20° Left - 10810190014704

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution

  • 10810190014704 ()
748221a

  • Cast cutting shears

Diver 20° Right - 10810190014698

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution

  • 10810190014698 ()
748211a

  • Cast cutting shears

Curette Bent 20° - 10810190018245

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution

  • 10810190018245 ()
904441t

  • Bone file/rasp, manual, reusable

Diver 20° Left - 10810190017927

No Description
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
B
In Commercial Distribution

  • 10810190017927 ()
748221t

  • Cast cutting shears

SUPERSONIC MACH 20 - 03760193600230

SUPERSONIC MACH 20
Supersonic Imagine, Inc.
SSIP95020-HOLX
In Commercial Distribution

  • 03760193600230 ()
SSIP95020-HOLX

  • General-purpose ultrasound imaging system

R.T.R.+ 80/20 - 03700501812870

Synthetic Bone Substitute Granules
BIOMATLANTE
RT0701M+GS50
In Commercial Distribution

  • 03700501812870 ()

  • Total Volume: 0.5 Milliliter
RT0701M+GS50

  • Bone matrix implant, synthetic, non-antimicrobial

NORMAL CONTROL (20) - 03607360047866

No Description
SEBIA
4786
In Commercial Distribution

  • 03607360047866 ()
4786

  • Protein electrophoresis IVD, control

HYPERGAMMA CONTROL (20) - 03607360047668

No Description
SEBIA
4766
In Commercial Distribution

  • 03607360047668 ()
4766

  • Protein electrophoresis IVD, control

LACRIJET® 20 - 03700773723256

A collection of devices intended to be used to maintain patency of the nasolacrimal system typically for treating/preventing pathologies of the tear drainage system (e.g., post-chemotherapy stenosis) or after dacryocystorhinostomy (DCR). It consists of a long and flexible bicanalicular or monocanalicular tube (e.g., Crawford type) inserted through the lacrimal puncta into the canaliculi, lacrimal sac, and/or nasolacrimal duct; devices to assist the intubation procedure are typically provided preassembled to the tube (e.g., cannula, probes, bougies, introducer, stylet). The tube is typically left in place long-term before removal. This is a single-use device.
FCI S A S FCI 20 22
S1.1522
In Commercial Distribution

  • 13700773723253 ()
  • 03700773723256 ()


  • Lacrimal intubation set

arcad® 20 - 03700879501048

Forceps
NOVASTEP
XFP03005
In Commercial Distribution

  • 03700879501048 ()
XFP03005

  • General internal orthopaedic fixation system implantation kit

arcad® 20 - 03700879500850

Drill Guide
NOVASTEP
XDG01005
In Commercial Distribution

  • 03700879500850 ()
XDG01005

  • General internal orthopaedic fixation system implantation kit

IMPLANT 20:1 - E27660437020

IMPLANT 20:1
SIRONA Dental Systems GmbH
6043702
Not in Commercial Distribution

  • E27660437020 ()


  • Dental surgical power tool motorized handpiece/set, pneumatic

EasyWinch 20 mm - 08058964727596

No Description
G21 SRL
900199
In Commercial Distribution

  • 08058964727596 ()


  • Balloon kyphoplasty kit

TETRIS ST 20° - 04047844114230

The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution

  • 04047844114230 ()

  • 15x10x32mm
TST20151032

  • Metallic spinal interbody fusion cage
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