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Disposable Vacuum Blood Collection Tube

by Henan Tuoren Medical Technology Co., Ltd. 425 variants

Ref BTSGH35, BTSGP45, BTSGM25, BTSGF95, BTSGE75, BTSPC08, BTSGI65, BTSGA00, BTSPN03, BTSPM00, BTSTH00, BTSGN08, BTSGF05, BTSPM05, BTSPF09, BTSGF55, BTSPK65, BTSGD08, BTSPD08, BTSPM08, BTSGF09, BTSGN04, BTSGK08, BTSPJ65, BTSGD45, BTSGJ03, BTSGP65, BTSGA85, BTSPK35, BTSPB95, BTSGJ55, BTSGK45, BTSGK85, BTSPP45, BTSPF00, BTSGP10, BTSGD07, BTSGK06, BTSPC95, BTSGB04, BTSPD65, BTSGB10, BTSPH07, BTSPP02, BTSGA95, BTSPD85, BTSPJ75, BTSPE03, BTSGG55, BTSGH25Model Sodium citrate 9:1, Sodium heparin/sodium fluoride, K2E/separation gel, Sodium heparin/separation gel, Sodium heparin, Coagulant/separation gel, Sodium citrate 4:1, No Additive, K3E/separation gel, K3EDTA, Lithium heparin, K2EDTA, Coagulant, Lithium heparin/separation gel

Active European Union

CE IVDR

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697575459084R3 Basic UDI-DI Date14 Dec 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / Reference
Sodium citrate 9:1, BTSGH35, Sodium heparin/sodium fluoride, BTSGP45, K2E/separation gel, BTSGM25, Sodium heparin/separation gel, BTSGF95, Sodium heparin, BTSGE75, Coagulant/separation gel, BTSPC08, Sodium citrate 4:1, BTSGI65, No Additive, BTSGA00, K3E/separation gel, BTSPN03, BTSPM00, BTSTH00, BTSGN08, BTSGF05, BTSPM05, BTSPF09, BTSGF55, K3EDTA, BTSPK65, Lithium heparin, BTSGD08, BTSPD08, BTSPM08, BTSGF09, BTSGN04, BTSGK08, K2EDTA, BTSPJ65, BTSGD45, BTSGJ03, BTSGP65, BTSGA85, BTSPK35, Coagulant, BTSPB95, BTSGJ55, BTSGK45, BTSGK85, BTSPP45, BTSPF00, BTSGP10, BTSGD07, BTSGK06, BTSPC95, BTSGB04, BTSPD65, BTSGB10, BTSPH07, BTSPP02, BTSGA95, BTSPD85, BTSPJ75, BTSPE03, Lithium heparin/separation gel, BTSGG55, BTSGH25
Primary DI / UDI-DI
06975754593594, 26975754596155, 06975754595390, 26975754592959, 06975754592559, 16975754592020, 06975754594218, 26975754590993, 06975754595949, 26975754595554, 06975754593518, 06975754595864, 16975754592860, 16975754595625, 06975754593129, 16975754592877, 16975754594932, 26975754592201, 06975754592382, 06975754595680, 26975754592942, 26975754595783, 26975754594786, 26975754594571, 06975754592139, 16975754594321, 06975754596199, 16975754591139, 16975754594871, 26975754591693, 06975754594379, 06975754594713, 26975754594793, 06975754596335, 16975754592976, 26975754596261, 06975754592184, 16975754594741, 26975754592058, 26975754591402, 16975754595397, 16975754592358, 06975754591521, 26975754593840, 26975754596285, 26975754591150, 06975754592399, 26975754594595, 06975754592641, 16975754593232, 26975754593574
Basic UDI-DI
697575459084R3, 697575459091QY, 697575459089RD, 697575459082QX, 697575459081QV, 697575459079RA, 697575459085R5, 697575459077R6, 697575459090QW, 697575459087R9, 697575459080QT, 697575459086R7, 697575459078R8, 697575459083QZ
EMDN Code
W050101010201, W050101010202
Device Class
Class A
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000017165
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

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Properties

  • Sterile
  • Professional Testing
  • New Device NoEUDAMEDYesEUDAMED

Other properties (8)

  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No