FDA UDI In Commercial Distribution 🇺🇸 United States

RECLAIM

DI: 10603295552857 · Model: 2999-67-015 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
RECLAIM
Primary DI
10603295552857
Version / Model
2999-67-015
Catalog Number
299967015
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-28
Public Version
1
Public Version Date
2025-08-05
Public Version Status
New
Public Device Record Key
32fd6b01-060d-4472-845c-ebd07b9b0e62

Device Description

RECLAIM TM MAKE TO ORDER NECK TRIAL SO

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
HWT TEMPLATE

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary 10603295552857

Customer Contacts