← Back to catalogue

Minitainer

FDA UDI

Class II (US FDA UDI)

by Tecomet, Inc

Identity

Trade Name
Minitainer FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
2 x 7 Base & Lid with 2 Silicone Strips for 2 Diamond Knives FDA UDI
Model / Reference
2 x 7 Base & Lid FDA UDI
Description
2 x 7 Base & Lid with 2 Silicone Strips for 2 Diamond Knives FDA UDI

Identifiers

Catalog Number
1-2720 FDA UDI
Primary DI / UDI-DI
00817766020025 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Device sterilization/disinfection container, reusable

Minitainer by Tecomet, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tecomet, Inc

Sources (1)

  • FDA UDI aded46a4-e9f3-46fb-a0dd-f40bcb1e0345 34 fields · synced Sep 18, 2026