FDA UDI In Commercial Distribution 🇺🇸 United States

RECLAIM

DI: 10603295156031 · Model: 2975-00-645 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RECLAIM
Primary DI
10603295156031
Version / Model
2975-00-645
Catalog Number
297500645
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
4
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
eece0f09-b1cb-4daa-961e-0633d27e1a14

Device Description

RECLAIM ASSEMBLY TENSILE BAR

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
64237 Orthopaedic implant inserter/extractor, single-use

Identifiers

Type ID
Primary 10603295156031

Customer Contacts