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Isodur®

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
Isodur® FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
ISODUR PROSTHESIS HEAD 12/14 36MM M FDA UDI
Model / Reference
NK670K FDA UDI
Description
ISODUR PROSTHESIS HEAD 12/14 36MM M FDA UDI

Identifiers

Catalog Number
NK670K FDA UDI
Primary DI / UDI-DI
04046963741136 FDA UDI
FDA Product Code
LZO FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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: Metallic femoral head prosthesis

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

Similar devices

Also classified as Metallic femoral head 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 e0fcc465-b99f-4f82-bf29-370fbdd1f5d3 36 fields · synced Jun 8, 2026