← Back to catalogue

2.4mm Locking Recon System

FDA UDI

Class I (US FDA UDI)

by Biomet Microfixation, Inc

Identity

Trade Name
2.4MM LOCKING RECON SYSTEM FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Model / Reference
24-4518T FDA UDI

Identifiers

Catalog Number
24-4518T FDA UDI
Primary DI / UDI-DI
00841036065348 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant template, reusable

2.4mm Locking Recon System by Biomet Microfixation, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, 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

Sources (1)

  • FDA UDI fe995c26-542b-4614-a630-e26d5fe2e7b7 34 fields · synced May 30, 2026