Identity
- Trade Name
- JAS Diagnostics FDA UDI
- Generic Name
- Alkaline phosphatase (ALP) isoenzyme IVD, kit, spectrophotometry FDA UDI
- Device Name
- ALP R2 (1x 30mL) UV FDA UDI
- Model / Reference
- ALP2-30R2U FDA UDI
- Description
- ALP R2 (1x 30mL) UV FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817274020722 FDA UDI
- FDA Product Code
- CJE FDA UDI
- GMDN Term
- Alkaline phosphatase (ALP) isoenzyme IVD, kit, spectrophotometry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1050 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
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: Alkaline phosphatase (ALP) isoenzyme IVD, kit, spectrophotometry
JAS Diagnostics by Drew Scientific , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Drew Scientific , Ltd.
Sources (1)
- FDA UDI 86fcc372-43fd-4e90-be9e-252f273b050e 35 fields · synced Jun 1, 2026