FDA UDI In Commercial Distribution 🇺🇸 United States

RECLAIM

DI: 10603295534839 · Model: 40-00000-41 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RECLAIM
Primary DI
10603295534839
Version / Model
40-00000-41
Catalog Number
400000041
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
2
Public Version Date
2023-04-10
Public Version Status
Update
Public Device Record Key
bf35c22a-d872-4188-8c74-d7ab9415115d

Device Description

RECLAIM MONOBLOC REVISION HIP SYSTEM MONOBLOC TRIAL EXTRACTOR

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
HWB EXTRACTOR

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 10603295534839

Customer Contacts