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Aia-Pack B12

FDA UDI

Class II (US FDA UDI)

by Tosoh Corp.

Identity

Trade Name
AIA-PACK B12 FDA UDI
Generic Name
Vitamin B12 IVD, kit, radioimmunoassay FDA UDI
Model / Reference
N/A FDA UDI

Identifiers

Primary DI / UDI-DI
14560189211879 FDA UDI
FDA Product Code
CDD FDA UDI
GMDN Term
Vitamin B12 IVD, kit, radioimmunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vitamin B12 IVD, kit, radioimmunoassay

Aia-Pack B12 by Tosoh Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitamin B12 IVD, kit, radioimmunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tosoh Corp.

Sources (1)

  • FDA UDI e3228c21-3418-44fb-9d54-58474d106ec4 34 fields · synced May 30, 2026