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Hermann Medizintechnik GmbH

FDA UDI

Class II (US FDA UDI)

by Hermann Medizintechnik GmbH

Identity

Trade Name
Hermann Medizintechnik GmbH FDA UDI
Generic Name
Electrosurgical handpiece, reusable FDA UDI
Device Name
Shaft insulated ø 5mm, WL 330mm FDA UDI
Model / Reference
H40-533-000 FDA UDI
Description
Shaft insulated ø 5mm, WL 330mm FDA UDI

Identifiers

Primary DI / UDI-DI
04059453003256 FDA UDI
510(k) Number
K051610 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Electrosurgical handpiece, 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical handpiece, 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 Electrosurgical handpiece, reusable.

Cleared under the same submission

K051610 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hermann Medizintechnik GmbH

Sources (1)

  • FDA UDI 669dbfd2-58b9-4e9c-a744-7204b16b21dd 35 fields · synced May 30, 2026