FDA UDI In Commercial Distribution 🇺🇸 United States

AGC TIBIAL PUNCH

DI: 05019279861941 · Model: 32-467284 · Biomet Uk Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AGC TIBIAL PUNCH
Primary DI
05019279861941
Version / Model
32-467284
Catalog Number
32-467284
Company Name
Biomet Uk Ltd
Labeler DUNS
219322575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-28
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8b721bc4-6e21-4890-9f8e-934e26c08b49

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWP PUNCH, FEMORAL NECK

GMDN Terms

Code Name
35287 Bone punch, reusable

Identifiers

Type ID
Primary 05019279861941

Customer Contacts