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SMR Resurfacing System

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR Resurfacing System FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
Gauge Dia.44mm FDA UDI
Model / Reference
Gauge FDA UDI
Description
Gauge Dia.44mm FDA UDI

Identifiers

Catalog Number
9013.27.044 FDA UDI
Primary DI / UDI-DI
08033390038522 FDA UDI
510(k) Number
K112900 FDA UDI
FDA Product Code
KWS FDA UDI
HSD FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3690 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

No

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

SMR Resurfacing System by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 31776a49-8719-4d76-b17b-2fdcc72b47b4 36 fields · synced Jun 8, 2026