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Mucotome

FDA UDI

Class I (US FDA UDI)

by Nouvag AG

Identity

Trade Name
Mucotome FDA UDI
Generic Name
Dermatome handpiece, electrically-powered FDA UDI
Device Name
Mucotome FDA UDI
Model / Reference
1970nou FDA UDI
Description
Mucotome FDA UDI

Identifiers

Primary DI / UDI-DI
ENOU1970NOU0 FDA UDI
FDA Product Code
GFD FDA UDI
GMDN Term
Dermatome handpiece, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dermatome handpiece, electrically-powered

Mucotome by Nouvag AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatome handpiece, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nouvag AG

Sources (1)

  • FDA UDI 2c994c33-8744-486b-abbb-9a5afc817488 34 fields · synced May 30, 2026