K-WIRE DEPTH GAUGE 13545

GUDID 00887868001710

Biomet Orthopedics, LLC

Surgical depth gauge, reusable
Primary Device ID00887868001710
NIH Device Record Key6649f50e-659b-4fd9-8405-42690031a508
Commercial Distribution StatusIn Commercial Distribution
Brand NameK-WIRE DEPTH GAUGE
Version Model Number13545
Catalog Number13545
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
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

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868001710 [Primary]

FDA Product Code

HTJGAUGE, DEPTH

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868001710]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-12-07
Device Publish Date2017-04-07

On-Brand Devices [K-WIRE DEPTH GAUGE]

008878680244672141-40-000
0088786800227414232
0088786800171013545
008878680494228241-98-000
0088786845823113545
00887868467240110018535

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