← Back to catalogue

Eti-Mak-2 Plus

FDA UDI

by Diasorin Inc.

Identity

Trade Name
ETI-MAK-2 PLUS FDA UDI
Generic Name
Hepatitis B virus surface antigen IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
P001932 FDA UDI

Identifiers

Primary DI / UDI-DI
08056771102377 FDA UDI
GMDN Term
Hepatitis B virus surface antigen IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hepatitis B virus surface antigen IVD, kit, enzyme immunoassay (EIA)

Eti-Mak-2 Plus by Diasorin Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hepatitis B virus surface antigen IVD, kit, enzyme immunoassay (EIA).

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
Diasorin Inc.

Sources (1)

  • FDA UDI b5fcb1b2-95cc-4b8e-a24c-f6d2f99a36d0 33 fields · synced May 30, 2026