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Aia-Pack Hcg Sample Diluting Solution

FDA UDI

Class II (US FDA UDI)

by Tosoh Corp.

Identity

Trade Name
AIA-PACK HCG SAMPLE DILUTING SOLUTION FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, reagent FDA UDI
Model / Reference
N/A FDA UDI

Identifiers

Primary DI / UDI-DI
04560189211841 FDA UDI
FDA Product Code
JHI FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 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: Total human chorionic gonadotropin IVD, reagent

Aia-Pack Hcg Sample Diluting Solution by Tosoh Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total human chorionic gonadotropin IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tosoh Corp.

Sources (1)

  • FDA UDI 7dbbdee7-014b-4f26-b9d7-12fffed58d0c 34 fields · synced Jun 8, 2026