FDA UDI In Commercial Distribution 🇺🇸 United States

Resolve Modular Revision Stem

DI: 04719886903393 · Model: 9104-3525 · UNITED ORTHOPEDIC CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Resolve Modular Revision Stem
Primary DI
04719886903393
Version / Model
9104-3525
Catalog Number
9104-3525
Company Name
UNITED ORTHOPEDIC CORP.
Labeler DUNS
656700556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-30
Public Version
1
Public Version Date
2024-09-09
Public Version Status
New
Public Device Record Key
044fa2b8-4111-4d67-949d-72fac0c50035

Device Description

Flexible reamer head, Ø25mm

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
Yes
PM Exempt
Yes
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
HTO Reamer

GMDN Terms

Code Name
35297 Medullary canal orthopaedic reamer, flexible

Identifiers

Type ID
Primary 04719886903393

Customer Contacts