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As Enduro

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AS ENDURO FDA UDI
Generic Name
Rotating hinged total knee prosthesis FDA UDI
Device Name
AS ENDURO MENISCAL COMPONENT F3 18MM FDA UDI
Model / Reference
NR894Z FDA UDI
Description
AS ENDURO MENISCAL COMPONENT F3 18MM FDA UDI

Identifiers

Catalog Number
NR894Z FDA UDI
Primary DI / UDI-DI
04046963937812 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

As 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 44874e5a-91eb-4e7d-bd50-ef881b866704 36 fields · synced Jun 8, 2026