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EliA Jo-1 Well

EUDAMEDFDA UDI

Class B (EU MDR)

Ref 14-5507-01

by Phadia AB

Identity

Trade Name
EliA Jo-1 Well EUDAMEDFDA UDI
Generic Name
Jo-1 antibody IVD, kit, fluorescent immunoassay FDA UDI
Device Name
EliA Jo-1 EUDAMED
EliA Jo-1 Well FDA UDI
Model / Reference
14-5507-01 EUDAMED
DECC055070 FDA UDI
Description
EliA Jo-1 Well FDA UDI

Identifiers

Catalog Number
DECC055070 FDA UDI
Primary DI / UDI-DI
07333066014586 EUDAMEDFDA UDI
Basic UDI-DI
7333066BUDI0076MF EUDAMED
FDA Product Code
LJM FDA UDI
EMDN Code
W0102100108 JO-1 EUDAMED
GMDN Term
Jo-1 antibody IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class B EUDAMED
Class II FDA UDI
Regulation Number
866.5100 FDA UDI
Market of Registration
Sweden 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

Yes

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

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

EliA Jo-1 Well by Phadia AB — Class B — 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
Phadia AB
EUDAMED SRN
SE-MF-000014170

Sources (2)

  • EUDAMED feaa5a51-401a-4177-b7c5-44d31a18aa64 61 fields · synced Jul 9, 2026
  • FDA UDI 14374215-3e79-433b-be33-152c0088392c 36 fields · synced May 29, 2026