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Autokit Micro Albumin

FDA UDI

Class I (US FDA UDI)

by Fujifilm Wako Pure Chemical Corporation

Identity

Trade Name
Autokit Micro Albumin FDA UDI
Generic Name
Albumin IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
In-Vitro Diagnostic Use FDA UDI
Model / Reference
999-06001 FDA UDI
Description
In-Vitro Diagnostic Use FDA UDI

Identifiers

Catalog Number
999-06001 FDA UDI
Primary DI / UDI-DI
04987481164666 FDA UDI
510(k) Number
K030320 FDA UDI
FDA Product Code
JIQ FDA UDI
GMDN Term
Albumin IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1645 FDA UDI
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

Yes

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: Albumin IVD, kit, nephelometry/turbidimetry

Autokit Micro Albumin by Fujifilm Wako Pure Chemical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Albumin IVD, kit, nephelometry/turbidimetry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78fa0a28-3246-4b80-a9eb-1f65f2cdc54a 37 fields · synced Jun 1, 2026