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T-Piv12

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref T-PIV12

by Kurin, Inc.

Identity

Trade Name
Kurin PIV (Peripheral IntraVenous) Connection, w/ Short Saf-T Holder Device FDA UDI
Generic Name
Blood collection set, invasive FDA UDI
Model / Reference
T-PIV12 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
20857606008145 EUDAMED
00857606008141 FDA UDI
Basic UDI-DI
B-20857606008145 EUDAMED
510(k) Number
K162233 FDA UDI
FDA Product Code
JKA FDA UDI
EMDN Code
W0501010201 CAPILLARY BLOOD COLLECTION SYSTEMS EUDAMED
GMDN Term
Blood collection set, invasive FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

T-Piv12 by Kurin, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kurin, Inc.
EUDAMED SRN
US-MF-000025001
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED b455db3f-c650-4399-87a9-c87f03f14760 61 fields · synced Jun 19, 2026
  • FDA UDI 3396260f-0cd0-45c7-b6e9-a6a4f730b7a3 33 fields · synced May 30, 2026