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SportMed Instruments

FDA UDI

Class I (US FDA UDI)

by Medacta International

Identity

Trade Name
SportMed Instruments FDA UDI
Generic Name
Arthroscopic access cannula, single-use FDA UDI
Device Name
Hip cannula System Ø6.1x90mm FDA UDI
Model / Reference
05.14.10.0020 FDA UDI
Description
Hip cannula System Ø6.1x90mm FDA UDI

Identifiers

Primary DI / UDI-DI
07630040725095 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Arthroscopic access cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Arthroscopic access cannula, single-use

SportMed Instruments by Medacta International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic access cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53c5fbfe-27af-466e-a6fd-d90abae72303 33 fields · synced May 30, 2026