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Enduro

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
ENDURO FDA UDI
Generic Name
Rotating hinged total knee prosthesis FDA UDI
Device Name
ENDURO FEMORAL COMPONENT CEMENTED F3L FDA UDI
Model / Reference
NB016K FDA UDI
Description
ENDURO FEMORAL COMPONENT CEMENTED F3L FDA UDI

Identifiers

Catalog Number
NB016K FDA UDI
Primary DI / UDI-DI
04046963165536 FDA UDI
FDA Product Code
KRO FDA UDI
GMDN Term
Rotating hinged total knee prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3510 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: Rotating hinged total knee prosthesis

Enduro by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotating hinged total knee prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 968c8c55-8459-439b-904b-0cfa53665607 36 fields · synced May 30, 2026