← Back to catalogue

HighSurg 30

FDA UDI

Class II (US FDA UDI)

by Nouvag AG

Identity

Trade Name
HighSurg 30 FDA UDI
Generic Name
Line-powered surgical power tool system motor FDA UDI
Device Name
Surgical motor system FDA UDI
Model / Reference
3365 FDA UDI
Description
Surgical motor system FDA UDI

Identifiers

Primary DI / UDI-DI
ENOU33650 FDA UDI
510(k) Number
K042434 FDA UDI
FDA Product Code
ERL FDA UDI
HBC FDA UDI
GMDN Term
Line-powered surgical power tool system motor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 FDA UDI
882.4360 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

No

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

HighSurg 30 by Nouvag AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Nouvag AG

Sources (1)

  • FDA UDI afdae9dd-e649-41cc-88cb-82a3e0f37cae 35 fields · synced May 30, 2026