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MNP Total Prosthesis Titanium

FDA UDI

Class II (US FDA UDI)

by Heinz Kurz

Identity

Trade Name
MNP Total Prosthesis Titanium FDA UDI
Generic Name
Ossicular prosthesis, total FDA UDI
Device Name
Ossicular Prosthesis, total FDA UDI
Model / Reference
1004440 FDA UDI
Description
Ossicular Prosthesis, total FDA UDI

Identifiers

Catalog Number
1004440 FDA UDI
Primary DI / UDI-DI
EHKM10044401 FDA UDI
510(k) Number
K972585 FDA UDI
FDA Product Code
ETA FDA UDI
GMDN Term
Ossicular prosthesis, total FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3495 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
MRI Safety
MR Conditional FDA UDI

Category: Ossicular prosthesis, total

MNP Total Prosthesis Titanium by Heinz Kurz — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ossicular prosthesis, total.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Heinz Kurz

Sources (1)

  • FDA UDI 17ccf949-b2ef-494a-8e73-a1a93ebb088c 36 fields · synced May 30, 2026