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MicroFrance® 7771B

by Integra Microfrance

Ref 7771B

MicroFrance® 7771B is a Class I device made by Integra Microfrance, registered in EUDAMED on 10 Jul 2026 (Basic UDI-DI 038178B0057CSS4A) and listed in FDA GUDID since 1 Sep 2017 (UDI-DI 10381780089032), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number038178B0057CSS4A Basic UDI-DI 10381780089032UDI-DIDate10 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10381780089032 UDI-DI Date1 Sep 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 038178B0057CSS4A registered 10 Jul 2026 Active
  • FDA GUDID UDI-DI 10381780089032 listed 1 Sep 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10381780089032
  2. Registered EUDAMED 038178B0057CSS4A

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
MicroFrance®
Generic name
Paranasal sinus guidewire
Device name
Accessory for Manual Instruments
Model / Ref / Catalog
7771B
Primary DI / UDI-DI
10381780089032
Basic UDI-DI
038178B0057CSS4A
Direct marketing DI
10381780089032
FDA product code
LRC
EMDN code
L149099 ENT instruments, reusable - other
GMDN term
Paranasal sinus guidewire
Device class
Class I
Regulation number
874.4420
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Paranasal sinus guidewire

Similar devices

Also classified as Paranasal sinus guidewire.

Similar devices in this category

Other devices filed under ENT INSTRUMENTS, REUSABLE - OTHER.

Other devices from Integra Microfrance

See all devices from Integra Microfrance →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)