REFOBACIN® BONE CEMENT R 110034357

GUDID 00880304990210

BIOMET

Orthopaedic cement, medicated
Primary Device ID00880304990210
NIH Device Record Keyb3ea1f7d-5426-4b50-9e5f-17d39cd1bff9
Commercial Distribution StatusIn Commercial Distribution
Brand NameREFOBACIN® BONE CEMENT R
Version Model Number110034357
Catalog Number110034357
Company DUNS260930126
Company NameBIOMET
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+0330475759100
Emaileufrvra@zimmerbiomet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304990210 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LODBONE CEMENT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-03-30

On-Brand Devices [REFOBACIN® BONE CEMENT R]

00880304990227110034358
00880304990210110034357
00880304990203110034356
00880304990197110034355

Trademark Results [REFOBACIN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
REFOBACIN
REFOBACIN
79023409 3245164 Dead/Cancelled
MERCK; Kommanditgesellschaft auf Aktien
2006-02-02
REFOBACIN
REFOBACIN
73323556 1290668 Dead/Cancelled
E. Merck
1981-08-13

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