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ReNew 3202

by Microline Surgical, Inc.

Part of a family of 30 devices: see the family page

Ref 3202

ReNew 3202 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 081109901DOC004SB) with CE/MDR certificate 3841767CE01 valid until 6 Sep 2031 and listed in FDA GUDID since 13 Jan 2020 (UDI-DI 00811099011361), 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 Number00811099011361 UDI-DI Date13 Jan 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 081109901DOC004SB registered 30 Jun 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00811099011361 listed 13 Jan 2020 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 00811099011361
  2. Registered EUDAMED 081109901DOC004SB
  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  • Withdrawn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 Traditional Grasper Tip EUDAMED
ReNew GUDID
Generic name
Rigid endoscopic tissue manipulation forceps, single-use
Device name
ReNew Disposable Tips
Model / Ref / Catalog
3202
Primary DI / UDI-DI
00811099011361
Basic UDI-DI
081109901DOC004SB
Unit of use DI
00811099011910
FDA product code
GEI
EMDN code
K0201010602 Laparoscopic and thoracoscopic electrosurgery forceps, single-use
GMDN term
Rigid endoscopic tissue manipulation forceps, single-use
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

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: Rigid endoscopic tissue manipulation forceps, single-use

Similar devices in this category

Other devices filed under ELECTROSURGERY FORCEPS, SINGLE-USE.

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

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)