914-0003

GUDID 00886385024516

Reduction Forceps

Stryker Trauma SA

Bone holding forceps Bone holding forceps
Primary Device ID00886385024516
NIH Device Record Key10c2bb6b-2bd6-4233-8773-913b96179e9c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number914-0003
Catalog Number914-0003
Company DUNS481999654
Company NameStryker Trauma SA
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100886385024516 [Primary]

FDA Product Code

HTDFORCEPS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00886385024516]

Moist Heat or Steam Sterilization


[00886385024516]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-08-21
Device Publish Date2018-09-21

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07613327415407 - PANGEA2024-03-11 Locking Screw
07613327415636 - PANGEA2024-03-11 Locking Screw

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