← Back to catalogue

Hermann Medizintechnik GmbH

FDA UDI

Class II (US FDA UDI)

by Hermann Medizintechnik GmbH

Identity

Trade Name
Hermann Medizintechnik GmbH FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Monopolar connection Umax: 4,3kVcable to laparoscopic instruments5m long to Hermann, Martin, Berchtoldunits FDA UDI
Model / Reference
H98-903-050 FDA UDI
Description
Monopolar connection Umax: 4,3kVcable to laparoscopic instruments5m long to Hermann, Martin, Berchtoldunits FDA UDI

Identifiers

Primary DI / UDI-DI
04059453026767 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical-only medical device connection cable, reusable

Hermann Medizintechnik GmbH by Hermann Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

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

Sources (1)

  • FDA UDI a79a3ff0-7912-403f-8514-e1c4eec6a252 34 fields · synced May 30, 2026