← Back to catalogue

Aia-Pack Rbc Folate

FDA UDI

Class II (US FDA UDI)

by Tosoh Corp.

Identity

Trade Name
AIA-PACK RBC FOLATE FDA UDI
Generic Name
Folate (vitamin B9) IVD, kit, radioimmunoassay FDA UDI
Model / Reference
N/A FDA UDI

Identifiers

Primary DI / UDI-DI
14560189212005 FDA UDI
FDA Product Code
CGN FDA UDI
GMDN Term
Folate (vitamin B9) IVD, kit, radioimmunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1295 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: Folate (vitamin B9) IVD, kit, radioimmunoassay

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

Similar devices

Also classified as Folate (vitamin B9) IVD, kit, radioimmunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tosoh Corp.

Sources (1)

  • FDA UDI d0a850da-899b-49c2-bd1d-562cdc3cff44 34 fields · synced May 31, 2026