Skip to content

ReNew 3151

by Microline Surgical, Inc.

Part of a family of 26 devices: see the family page

Ref 3151

ReNew 3151 is a device classified as Class IIb in the EU and Class II in the US made by Microline Surgical, Inc., registered in EUDAMED on 30 Jun 2026 (Basic UDI-DI 081109901DOC005SD) with CE/MDR certificate 3841767CE01 valid until 6 Sep 2031 and listed in FDA GUDID since 13 Nov 2017 (UDI-DI 00811099014010), active as of 22 Oct 2026.

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

CE MDR

Valid until

6 Sep 2031

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

1 certificate

Certifier DEKRA Certification B.V.

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number3841767CE01 Date6 Sep 2026IssuedStatusActive expires 6 Sep 2031
United StatesGUDID listing GUDID Number00811099014010 UDI-DI Date13 Nov 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 081109901DOC005SD registered 30 Jun 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00811099014010 listed 13 Nov 2017 Listed

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 3841767CE01 Active Reissued

    Quality management system EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    6 Sep 2026
    Expires
    6 Sep 2031

Timeline

4 dated events

  1. Listed FDA GUDID 00811099014010
  2. Registered EUDAMED 081109901DOC005SD
  3. Certificate issued EUDAMED 3841767CE01
  4. Certificate expires EUDAMED 3841767CE01

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  • Withdrawn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
ReNew Mini Endocut Scissor EUDAMED
ReNew GUDID
Generic name
Flexible endoscopic scissors, reusable
Device name
ReNew Reusable Tips
Model / Ref / Catalog
3151
Primary DI / UDI-DI
00811099014010 EUDAMED
00811099011897 GUDID
Basic UDI-DI
081109901DOC005SD
Direct marketing DI
00811099014010
FDA product code
GEI
EMDN code
L1204 Laparoscopic and thoracoscopic surgery forceps, reusable
GMDN term
Flexible endoscopic scissors, reusable
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.4400
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00811099014010
GUDID
00811099011897
Device classEUDAMED
Class IIb
GUDID
Class II

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00811099014010; FDA GUDID lists 00811099011897), so their flags are not compared. Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Flexible endoscopic scissors, reusable

Similar devices in this category

Other devices filed under LAPAROSCOPIC AND THORACOSCOPIC SURGERY FORCEPS, REUSABLE.

Other devices from Microline Surgical, Inc.

  • ReNew 3412

    Class II

  • ReNew 3362

    Class II

  • ReNew 3946

    Class II

  • ReNew 3411

    Class II

See all devices from Microline Surgical, Inc. →

Properties

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