Tecomet

FDA UDI

Class I (US FDA UDI)

by Tecomet, Inc

Identity

Trade Name: Tecomet FDA UDI
Generic Name: Bone lever/elevator, reusable FDA UDI
Device Name: Bone Probe, Straight Palm Impactor .125W, Small Taper 9.53", Black FDA UDI
Model / Reference: BP101001-A FDA UDI
Description: Bone Probe, Straight Palm Impactor .125W, Small Taper 9.53", Black FDA UDI

Identifiers

Primary DI / UDI-DI: 00818069015923 FDA UDI
FDA Product Code: HXB FDA UDI
GMDN Term: Bone lever/elevator, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone lever/elevator, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Tecomet, Inc

Sources (1)

FDA UDI 49c1874f-0c93-466f-af25-dd4b17f31870 33 fields · synced Sep 18, 2026