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Gimmi

FDA UDI

Class II (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Electrosurgical handpiece, reusable FDA UDI
Device Name
ALPHAACTIVEGRIP SHAFT Ø 5 MM, FOR ERGO RINGHANDLE WORKING LENGTH 340 MM FDA UDI
Model / Reference
T.0052.14 FDA UDI
Description
ALPHAACTIVEGRIP SHAFT Ø 5 MM, FOR ERGO RINGHANDLE WORKING LENGTH 340 MM FDA UDI

Identifiers

Catalog Number
T.0052.14 FDA UDI
Primary DI / UDI-DI
04049047127710 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Electrosurgical handpiece, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical handpiece, reusable

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

Similar devices

Also classified as Electrosurgical handpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (1)

  • FDA UDI 2d1a21f2-6cc1-4b89-ad4f-62f76aa7c88a 35 fields · synced May 30, 2026