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DUFNER Instrumente GmbH

FDA UDI

Class II (US FDA UDI)

by DUFNER - Instrumente GmbH Fabrik ärztlicher Instrumente Medizintechnik

Identity

Trade Name
DUFNER Instrumente GmbH FDA UDI
Generic Name
Endoscope suction valve, reusable FDA UDI
Device Name
MICTEC Suction tube without basket, big central opening, 30° curved, Ø 4.5 mm, 300 mm working length FDA UDI
Model / Reference
20943-04 FDA UDI
Description
MICTEC Suction tube without basket, big central opening, 30° curved, Ø 4.5 mm, 300 mm working length FDA UDI

Identifiers

Primary DI / UDI-DI
04063763200601 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscope suction valve, 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscope suction valve, reusable

DUFNER Instrumente GmbH by DUFNER - Instrumente GmbH Fabrik ärztlicher Instrumente Medizintechnik — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Endoscope suction valve, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 23c37da8-1e67-400a-9528-0168786d3e09 34 fields · synced Jun 8, 2026