FDA UDI In Commercial Distribution 🇺🇸 United States

Tecomet

DI: 00818069018092 · Model: RC302002-J · TECOMET INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tecomet
Primary DI
00818069018092
Version / Model
RC302002-J
Company Name
TECOMET INC.
Labeler DUNS
078749695
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-08
Public Version
1
Public Version Date
2020-10-16
Public Version Status
New
Public Device Record Key
202162b3-6bf6-47ed-b591-cc7897a739d3

Device Description

Table Top Rod Cutter, 4.76-5.50-6.35 Collapsible/Removeable Drain Hole, Blue

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
FZT Cutter, Surgical

GMDN Terms

Code Name
44805 Orthopaedic implantable-device cutter

Identifiers

Type ID
Primary 00818069018092