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DIABJET2

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Part of a family of 19 devices: see the family page

Ref PA2 30GModel PA PA2 NPA APA

DIABJET2 (PA2 30G) is a Class IIa device made by Shandong Lianfa Medical Plastic Products Co., Ltd., registered in EUDAMED on 15 May 2024 (Basic UDI-DI 69495170PAHH), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69495170PAHH Basic UDI-DI 06949517010703UDI-DIDate15 May 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
safety lancets
Model / reference
PA PA2 NPA APA, PA2 30G
Primary DI / UDI-DI
06949517010703
Basic UDI-DI
69495170PAHH
EMDN code
V010401 Lancets with safety systems, single-use
Device class
Class IIa
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000028790
Authorised representative
Linkfar Healthcare GmbH DE-AR-000005107

Similar devices in this category

Other devices filed under LANCETS WITH SAFETY SYSTEMS, SINGLE-USE.

Other devices from Shandong Lianfa Medical Plastic Products Co., Ltd.

See all devices from Shandong Lianfa Medical Plastic Products Co., Ltd. →

Properties

  • Supplied sterile
Other properties (13, all answered No)