Gluceofine Pro
by Shandong Lianfa Medical Plastic Products Co., Ltd.
Part of a family of 19 devices: see the family page
Ref PA 28GModel PA PA2 NPA APA
Gluceofine Pro (PA 28G) 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
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69495170PAHH 06949517009998 | Date15 May 2024 | StatusActive |
Official records
- EUDAMED public site 69495170PAHH
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- safety lancets
- Model / reference
- PA PA2 NPA APA, PA 28G
- Primary DI / UDI-DI
- 06949517009998
- 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
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000028790
- Authorised representative
- Linkfar Healthcare GmbH DE-AR-000005107
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