Skip to content

Safety venous blood collection needle for single use

by Chengdu Puth Medical Technology Co., Ltd. 14 variants

Ref 694799002668, 694799002602, 694799002644, 694799002645, 694799002670, 694799002653, 694799002605, 694799002652, 694799002649, 694799002667, 694799002664, 694799002661, 694799002541, 694799002671, 694799002603, 694799002672, 694799002669Model Flash-back with Window type (AQKJ), Soft tube Type（AQRJ）, Pen Type (AQZT), Pen Type (ZT)

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69479900AQCXZ/AQKJLV Basic UDI-DI Date14 Sep 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
Safety venous blood collection needle for single use
Venous blood collection needles for single use
Model / Reference
Flash-back with Window type (AQKJ), 694799002668, Soft tube Type（AQRJ）, 694799002602, Pen Type (AQZT), 694799002644, 694799002645, 694799002670, 694799002653, 694799002605, 694799002652, 694799002649, 694799002667, 694799002664, 694799002661, Pen Type (ZT), 694799002541, 694799002671, 694799002603, 694799002672, 694799002669
Primary DI / UDI-DI
06947990026686, 06947990026020, 06947990026440, 06947990026457, 06947990026709, 06947990026532, 06947990026051, 06947990026525, 06947990026495, 06947990026679, 06947990026648, 06947990026617, 06947990025412, 06947990026716, 06947990026037, 06947990026723, 06947990026693
Basic UDI-DI
69479900AQCXZ/AQKJLV, 69479900AQCXZ/AQRJMJ, 69479900AQCXZ/AQZTNW, 69479900CXZ/ZT5X
Unit of Use DI
16947990026683, 16947990026027, 16947990026447, 16947990026454, 16947990026706, 16947990026539, 16947990026058, 16947990026522, 16947990026492, 16947990026676, 16947990026645, 16947990026614, 16947990025419, 16947990026713, 16947990026034, 16947990026720, 16947990026690
EMDN Code
A01010501, A01010502
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000005947
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Chengdu Puth Medical Technology Co., Ltd.

See all devices from Chengdu Puth Medical Technology Co., Ltd. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No