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Gimmi

FDA UDI

Class II (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Insufflation gas conditioning tubing set FDA UDI
Device Name
SINGLE USE HEATING TUBE FOR S.2959.00 INSUFFLATION TUBE HIGH-FLOW, WITH HEATING AND HYGIENIC FILTER FDA UDI
Model / Reference
S.2959.20 FDA UDI
Description
SINGLE USE HEATING TUBE FOR S.2959.00 INSUFFLATION TUBE HIGH-FLOW, WITH HEATING AND HYGIENIC FILTER FDA UDI

Identifiers

Catalog Number
S.2959.20 FDA UDI
Primary DI / UDI-DI
04049047666141 FDA UDI
FDA Product Code
HIF FDA UDI
GMDN Term
Insufflation gas conditioning tubing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Insufflation gas conditioning tubing set

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

Similar devices

Also classified as Insufflation gas conditioning tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (1)

  • FDA UDI 0837783c-79f2-479f-8c89-b49295c1bd30 35 fields · synced May 30, 2026