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Coag-Sense Prothrombin Time (PT)/INR Test Strip Kit

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 03P56-50Model 100218

by CoaguSense Inc.

Identity

Trade Name
Coag-Sense Prothrombin Time (PT)/INR Test Strip Kit EUDAMED
Coag-Sense Test Strip Kit, 50 ct. FDA UDI
Generic Name
Prothrombin time (PT) IVD, kit, rapid clotting, clinical FDA UDI
Device Name
Coag-Sense Prothrombin Time (PT)/INR Test Strip Kit - 50 Count EUDAMED
Test Strip Kit, 50 ct. FDA UDI
Model / Reference
100218 EUDAMEDFDA UDI
03P56-50 EUDAMED
Description
Test Strip Kit, 50 ct. FDA UDI

Identifiers

Catalog Number
03P56-50 FDA UDI
Primary DI / UDI-DI
00861900000398 EUDAMEDFDA UDI
Basic UDI-DI
B-00861900000398 EUDAMED
FDA Product Code
GJS FDA UDI
EMDN Code
W0103020101 PROTHROMBIN TIME ( QUICK TEST ) EUDAMED
GMDN Term
Prothrombin time (PT) IVD, kit, rapid clotting, clinical FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
864.7750 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Coag-Sense Prothrombin Time (PT)/INR Test Strip Kit by CoaguSense Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CoaguSense Inc.
EUDAMED SRN
US-MF-000026989
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 871a9708-05f1-45fc-b206-aade8abd059e 61 fields · synced Jun 19, 2026
  • FDA UDI 11a189f9-f850-4f7f-ad53-8d5a6ab702a0 36 fields · synced May 30, 2026