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DemeLENE PM193019F4P

by DemeTECH Corp

Ref PM193019F4P

DemeLENE PM193019F4P is a device classified as Class IIb in the EU and Class II in the US made by DemeTECH Corp, registered in EUDAMED on 10 Jul 2026 (Basic UDI-DI B-10652927195382), cleared under FDA 510(k) K043330 on 16 May 2005 and listed in FDA GUDID since 19 Oct 2016 (UDI-DI 10652927195382), active as of 23 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K043330

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10652927195382 Basic UDI-DI 10652927195382UDI-DIDate10 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10652927195382 UDI-DI Date19 Oct 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK043330 Date16 May 2005DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-10652927195382 registered 10 Jul 2026 Active
  • FDA 510(k) K043330 decided 16 May 2005 Active
  • FDA GUDID UDI-DI 10652927195382 listed 19 Oct 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K043330
  2. Listed FDA GUDID 10652927195382
  3. Registered EUDAMED B-10652927195382

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
DemeLENE
Generic name
Polyolefin/fluoropolymer suture, monofilament
Model / reference
PM193019F4P
Description
Synthetic, Monofilament , Nonabsorbable Suture
Primary DI / UDI-DI
10652927195382
Basic UDI-DI
B-10652927195382
510(k) Number
FDA product code
GAW
EMDN code
H010201010401 Polypropylene monofilament with needle for open surgery
GMDN term
Polyolefin/fluoropolymer suture, monofilament
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.5010
EU registration type
Legacy device (under a directive)
EU market of registration
Hungary
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: Polyolefin/fluoropolymer suture, monofilament

Cleared under the same submission (K043330)

and 8 more cleared under K043330

Similar devices in this category

Other devices filed under POLYPROPYLENE MONOFILAMENT WITH NEEDLE FOR OPEN SURGERY.

Other devices from DemeTECH Corp

See all devices from DemeTECH Corp →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)