Lactosorb* 2.0mm System

FDA UDI

Class I (US FDA UDI)

by Biomet Microfixation, Inc

Identity

Trade Name: LACTOSORB* 2.0MM SYSTEM FDA UDI
Generic Name: Bone tap, single-use, non-sterile FDA UDI
Model / Reference: 915-2074 FDA UDI

Identifiers

Catalog Number: 915-2074 FDA UDI
Primary DI / UDI-DI: 00841036054298 FDA UDI
FDA Product Code: HWX FDA UDI
GMDN Term: Bone tap, single-use, non-sterile 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

Yes

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone tap, single-use, non-sterile

Lactosorb* 2.0mm System by Biomet Microfixation, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, single-use, non-sterile.

TAP, CANCELLOUS, SOLID, S-COUPLE — Biomet Orthopedics, Inc. · Class I
SOLID CANCELLOUS TAP — Biomet Orthopedics, Inc. · Class I
ORTHOSORB LS2.0 mm STRAIGHT PIN KIT, 1 PIN — Biomet Orthopedics, Inc. · Class II
CANNULATED CANCELLOUS TAP — Biomet Orthopedics, Inc. · Class I
FuzeFix Large — FUSION ORTHOPEDICS, LLC · Class II
CANNULATED CANCELLOUS TAP — Biomet Orthopedics, Inc. · Class I
AOS CORTICAL TAP, LARGE HUDSON 5.0mm — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I
AOS CALIBRATED CORTICAL TAP 6.5mm — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I

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

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

Manufacturer

Manufacturer: Biomet Microfixation, Inc

Sources (1)

FDA UDI 478a0e0c-4435-49df-b70f-db59f449f9b3 34 fields · synced Jun 8, 2026