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Capillarys / Minicap Wash Solution (2)

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 2052

by sebia

Identity

Trade Name
CAPILLARYS / MINICAP WASH SOLUTION (2) EUDAMED
CAPILLARYS/MINICAP WASH SOLUTION (2) FDA UDI
Generic Name
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI
Device Name
CAPILLARYS / MINICAP WASH SOLUTION (2) EUDAMED
CAPILLARYS /MINICAP WASH SOLUTION IS USED IN CONJUNCTION WITH 510K CLEARED KITS. THE SOLUTION WAS PART OF THE PERFORMANCE TESTING INCLUDED WITH K082085. FDA UDI
Model / Reference
2052 EUDAMEDFDA UDI
Description
CAPILLARYS /MINICAP WASH SOLUTION IS USED IN CONJUNCTION WITH 510K CLEARED KITS. THE SOLUTION WAS PART OF THE PERFORMANCE TESTING INCLUDED WITH K082085. FDA UDI

Identifiers

Catalog Number
2052 FDA UDI
Primary DI / UDI-DI
03607360020524 EUDAMEDFDA UDI
Basic UDI-DI
3607362052BUBP EUDAMED
FDA Product Code
CEF FDA UDI
EMDN Code
W01010499 MULTIPLE CLIN. CHEM LAB REAGENTS - OTHER EUDAMED
GMDN Term
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.1630 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Capillarys / Minicap Wash Solution (2) by Sebia — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
sebia
EUDAMED SRN
FR-MF-000003520

Sources (2)

  • EUDAMED 51d8a9d3-f7b0-4979-a406-c7a8716adaea 61 fields · synced Jul 16, 2026
  • FDA UDI a700fba6-f2b4-4964-a02c-9e97367df170 35 fields · synced May 30, 2026