FDA UDI In Commercial Distribution 🇺🇸 United States

TAPERLOC COMPLETE RASP/PROVISIONAL

DI: 00880304529687 · Model: 51-203200 · Biomet Orthopedics, LLC
Product Codes
8
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TAPERLOC COMPLETE RASP/PROVISIONAL
Primary DI
00880304529687
Version / Model
51-203200
Catalog Number
51-203200
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-28
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
6b5865d7-d0ef-4112-a2d7-bc9150709dc6

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
KWL Prosthesis, hip, hemi-, femoral, metal
MEH Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00880304529687

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120030 000