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Tecomet

FDA UDI

Class I (US FDA UDI)

by Tecomet, Inc

Identity

Trade Name
Tecomet FDA UDI
Generic Name
Bone trephine, reusable FDA UDI
Device Name
Reamer Assembly, Hollow 7mm 1/4" Male Square Drive FDA UDI
Model / Reference
HR1012756 FDA UDI
Description
Reamer Assembly, Hollow 7mm 1/4" Male Square Drive FDA UDI

Identifiers

Primary DI / UDI-DI
00818069010928 FDA UDI
FDA Product Code
HWB FDA UDI
GMDN Term
Bone trephine, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone trephine, reusable

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

Similar devices

Also classified as Bone trephine, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tecomet, Inc

Sources (1)

  • FDA UDI d93b405c-73d9-4d84-ac73-24658f9338ea 33 fields · synced Sep 18, 2026