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Smr Stemless

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
SMR STEMLESS FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
SMR STEMLESS - Reamer Shaft FDA UDI
Model / Reference
9013.55.039 FDA UDI
Description
SMR STEMLESS - Reamer Shaft FDA UDI

Identifiers

Catalog Number
9013.55.039 FDA UDI
Primary DI / UDI-DI
08033390108065 FDA UDI
FDA Product Code
HSD FDA UDI
KWT FDA UDI
PHX FDA UDI
KWS FDA UDI
PAO FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
888.3650 FDA UDI
888.3660 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 instrument handle, non-torque-limiting

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

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 24d3069e-23aa-46f8-8eb7-3fcd49775b7c 34 fields · synced Jun 1, 2026