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Drill Measuring Sleeve

FDA UDI

Class I (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
DRILL MEASURING SLEEVE FDA UDI
Generic Name
Orthopaedic implantation sleeve, single-use FDA UDI
Model / Reference
2112-01-410 FDA UDI

Identifiers

Catalog Number
211201410 FDA UDI
Primary DI / UDI-DI
00887868023415 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implantation sleeve, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic implantation sleeve, single-use

Drill Measuring Sleeve by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantation sleeve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Orthopedics, Inc.

Sources (1)

  • FDA UDI 96557198-da39-4864-81b4-f7dac9e2a70e 35 fields · synced Jun 8, 2026