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Prima

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
PRIMA FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
PRIMA - Impactor Adaptor #1 FDA UDI
Model / Reference
9013.67.141 FDA UDI
Description
PRIMA - Impactor Adaptor #1 FDA UDI

Identifiers

Catalog Number
9013.67.141 FDA UDI
Primary DI / UDI-DI
08033390216470 FDA UDI
FDA Product Code
HSD FDA UDI
KWT FDA UDI
PHX FDA UDI
KWS FDA UDI
PAO FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable 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: Orthopaedic prosthesis implantation positioning instrument, reusable

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

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI d3d99fd6-2dbf-4cca-95b6-5653efc07d5c 35 fields · synced Jun 8, 2026