FDA UDI In Commercial Distribution 🇺🇸 United States

RECLAIM

DI: 10603295533641 · Model: 10-235-4523 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RECLAIM
Primary DI
10603295533641
Version / Model
10-235-4523
Catalog Number
102354523
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-28
Public Version
1
Public Version Date
2023-04-05
Public Version Status
New
Public Device Record Key
520a9087-c892-4ea1-82b4-fdd6911a1f86

Device Description

RECLAIM MONOBLOC REVISION FEMORAL STEM LONG STEM HIGH OFFSET HO 23 CEMENTLESS

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
55834 Press-fit hip femur prosthesis, one-piece

Identifiers

Type ID
Primary 10603295533641

Customer Contacts