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Tcm 3000 Bl

FDA UDI

Class I (US FDA UDI)

by Nouvag AG

Identity

Trade Name
TCM 3000 BL FDA UDI
Generic Name
Line-powered surgical power tool system motor FDA UDI
Device Name
Surgical motor system FDA UDI
Model / Reference
3285 FDA UDI
Description
Surgical motor system FDA UDI

Identifiers

Primary DI / UDI-DI
ENOU32850 FDA UDI
FDA Product Code
GEY FDA UDI
GMDN Term
Line-powered surgical power tool system motor 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: Line-powered surgical power tool system motor

Tcm 3000 Bl by Nouvag AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Line-powered surgical power tool system motor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nouvag AG

Sources (1)

  • FDA UDI 1f79252b-7909-4ff6-b54a-4a405af19eb7 34 fields · synced May 30, 2026