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SMR Shoulder system

FDA UDI

Class I (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR Shoulder system FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
Short M6 Aligment Rod FDA UDI
Model / Reference
9CCA.13.018 FDA UDI
Description
Short M6 Aligment Rod FDA UDI

Identifiers

Catalog Number
9CCA.13.018 FDA UDI
Primary DI / UDI-DI
08033390115766 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical implant template, 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

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

SMR Shoulder system by Limacorporate — 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

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 3addfd9b-a497-4fcb-81f8-e9eee6331593 35 fields · synced Jun 6, 2026