FDA UDI In Commercial Distribution 🇺🇸 United States

CeMend Reamer 14mm

DI: 08058964729309 · Model: AR-902-17 · G21 SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
CeMend Reamer 14mm
Primary DI
08058964729309
Version / Model
AR-902-17
Company Name
G21 SRL
Labeler DUNS
431529195
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-19
Public Version
1
Public Version Date
2025-12-29
Public Version Status
New
Public Device Record Key
ac7a684a-7e9a-43be-8d6f-d51f75eebc50

Device Description

Reamer with diameter 14mm

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
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
63526 Shoulder revision prosthesis trial

Identifiers

Type ID
Primary 08058964729309