← Back to catalogue

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
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
MICTEC Biopsy forceps, pistol grip, with cleaning flush port, Ø 2.0 mm, 240 mm working length FDA UDI
Model / Reference
27996-01 FDA UDI
Description
MICTEC Biopsy forceps, pistol grip, with cleaning flush port, Ø 2.0 mm, 240 mm working length FDA UDI

Identifiers

Primary DI / UDI-DI
04063763178986 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid endoscopic biopsy forceps, 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: Rigid endoscopic biopsy forceps, 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 Rigid endoscopic biopsy forceps, reusable.

Cleared under the same submission

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 93e9181f-f92c-4de7-89ae-c383c78d3aad 34 fields · synced Jun 1, 2026