SELF HOLDING SCREW FORCEPS 939999262

GUDID 00887868446474

Biomet Orthopedics, LLC

Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps
Primary Device ID00887868446474
NIH Device Record Keyf6e2b2ac-25fc-4008-8c81-1f90b9a99bc8
Commercial Distribution StatusIn Commercial Distribution
Brand NameSELF HOLDING SCREW FORCEPS
Version Model Number939999262
Catalog Number939999262
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
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]
GS100887868446474 [Primary]

FDA Product Code

HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING
HYAFORCEPS, WIRE HOLDING

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


[00887868446474]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-14
Device Publish Date2020-09-04

On-Brand Devices [SELF HOLDING SCREW FORCEPS]

00887868067792939999262
00887868446474939999262

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.