FDA UDI In Commercial Distribution 🇺🇸 United States

Arcos® Revision Hip Instrumentation

DI: 05019279431526 · Model: 31-301918 · Biomet Uk Ltd
Product Codes
7
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Arcos® Revision Hip Instrumentation
Primary DI
05019279431526
Version / Model
31-301918
Catalog Number
31-301918
Company Name
Biomet Uk Ltd
Labeler DUNS
219322575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-08
Public Version
3
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
9e9ca5e7-4a05-413c-860f-520f5d76a338

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
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
MAY Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish
MEH Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 05019279431526

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K100469 000