FDA UDI In Commercial Distribution 🇺🇸 United States

Tecomet

DI: 00841435121850 · Model: 7967029 · TECOMET INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tecomet
Primary DI
00841435121850
Version / Model
7967029
Company Name
TECOMET INC.
Labeler DUNS
078749695
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-17
Public Version
1
Public Version Date
2023-05-25
Public Version Status
New
Public Device Record Key
3436d1b0-35f7-49db-819d-f69a83706f07

Device Description

SYPERT RONGEUR 14 1/2" 8X16MM

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
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
HTX Rongeur

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00841435121850