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.
- Optilite Albumin Kit — The Binding Site Group · Class II
- N Antiserum to Human Albumin — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class II
- Atellica CH Alb — Siemens Healthcare Diagnostics · Class II
- ADVIA® Chemistry Albumin, ALB_c Albumin Reagents, Concentrated — Siemens Healthcare Diagnostics · Class II
- Yumizen C1200 Albumin U/CSF — Horiba Abx · Class II
- Atellica CH Urine Albumin (UAlb) — Siemens Healthcare Diagnostics · Class II
- Microalbuminuria Kit (Immunoturbidimetric Method) — Medicalsystem Biotechnology Co., Ltd. · Class II
- ADVIA® Chemistry ALB Albumin BCG Reagents — Siemens Healthcare Diagnostics · Class II
Cleared under the same submission
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fujifilm Wako Pure Chemical Corporation
Sources (1)
- FDA UDI 78fa0a28-3246-4b80-a9eb-1f65f2cdc54a 37 fields · synced Jun 1, 2026