FDA UDI In Commercial Distribution 🇺🇸 United States

Tecomet

DI: 00841435100176 · Model: LC50001 · TECOMET INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Tecomet
Primary DI
00841435100176
Version / Model
LC50001
Company Name
TECOMET INC.
Labeler DUNS
078749695
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-02
Public Version
2
Public Version Date
2026-02-17
Public Version Status
Update
Public Device Record Key
ab940d83-9683-485b-8916-f3b1c885e37d

Device Description

2nd Generation Evolution Lid Thoracolumbar Blank

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
No
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
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 00841435100176
Previous 00818069019013

Customer Contacts

Phone
262-925-4531

Premarket Submissions

Submission Number Supplement Number
K012105 000