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Aia-Pack B12 Pretreatment Set

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 0020706

by Tosoh Corporation

Identity

Trade Name
AIA-PACK B12 Pretreatment Set FDA UDI
Generic Name
Vitamin B12 IVD, reagent FDA UDI
Device Name
AIA-PACK B12 PRETREATMENT SET EUDAMED
Model / Reference
0020706 EUDAMED
N/A FDA UDI

Identifiers

Primary DI / UDI-DI
04560189211896 EUDAMEDFDA UDI
Basic UDI-DI
B-04560189211896 EUDAMED
FDA Product Code
CDD FDA UDI
EMDN Code
W0102070204 VITAMIN B12 EUDAMED
GMDN Term
Vitamin B12 IVD, reagent FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
862.1810 FDA UDI
Market of Registration
Belgium 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

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

Prescription Use

No

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

Aia-Pack B12 Pretreatment Set by Tosoh Corporation — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tosoh Corporation
EUDAMED SRN
JP-MF-000024143
Authorised Representative
Tosoh Europe N.V. BE-AR-000000211

Sources (2)

  • EUDAMED fdf57cbe-bc8f-49cd-b980-39ace639bc37 61 fields · synced Jun 18, 2026
  • FDA UDI 5bc746c2-a79b-43fd-9f39-ca95e230a149 34 fields · synced May 30, 2026