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Smr Stemless

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR STEMLESS FDA UDI
Generic Name
Humeral head spacer FDA UDI
Device Name
SSMR STEMLESS - 2MM ECCENTRICAL ADAPTOR WITH SCREW FDA UDI
Model / Reference
1335.15.202 FDA UDI
Description
SSMR STEMLESS - 2MM ECCENTRICAL ADAPTOR WITH SCREW FDA UDI

Identifiers

Catalog Number
1335.15.202 FDA UDI
Primary DI / UDI-DI
08033390107730 FDA UDI
FDA Product Code
PKC FDA UDI
GMDN Term
Humeral head spacer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Humeral head spacer

Smr Stemless by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Humeral head spacer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 641e7a05-579e-4d13-96d6-4adf6ca0f389 35 fields · synced Jun 8, 2026