Identity
- Trade Name
- Amazewell FDA UDI
- Generic Name
- Barbiturate IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- Amazewell™ Multi-Drug Urine Test Clicker Cup, 12-Panel, 25T/Box FDA UDI
- Model / Reference
- ASUD-3124 FDA UDI
- Description
- Amazewell™ Multi-Drug Urine Test Clicker Cup, 12-Panel, 25T/Box FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850054867254 FDA UDI
- 510(k) Number
- K232659 FDA UDI
- FDA Product Code
- NFV FDA UDINGL FDA UDIPTH FDA UDINFT FDA UDINFY FDA UDIPTG FDA UDINGG FDA UDINGM FDA UDINFW FDA UDIQBF FDA UDIDJG FDA UDIQAW FDA UDI
- GMDN Term
- Barbiturate IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3170 FDA UDI862.3650 FDA UDI862.3150 FDA UDI862.3100 FDA UDI862.3250 FDA UDI862.3620 FDA UDI862.3610 FDA UDI862.3870 FDA UDI862.3700 FDA UDI862.3910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
Yes
Implantable
No
Contains Latex
No
Prescription Use
No
Over-the-Counter
Yes
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
No
Category: Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinicalCocaine/cocaine metabolite IVD, kit, rapid ICT, clinicalOpiate/opiate metabolite IVD, kit, rapid ICT, clinicalAmphetamine-specific IVD, kit, rapid ICT, clinical
Amazewell by Guangzhou Decheng Biotechnology Co., LTD — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Propoxyphene/propoxyphene metabolite IVD, kit, rapid ICT, clinical.
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Cleared under the same submission
K232659 also covers:
- AllSource — Guangzhou Decheng Biotechnology Co., LTD
- AllSource — Guangzhou Decheng Biotechnology Co., LTD
- AllSource — Guangzhou Decheng Biotechnology Co., LTD
- AllSource — Guangzhou Decheng Biotechnology Co., LTD
- AllSource — Guangzhou Decheng Biotechnology Co., LTD
- Amazewell — Guangzhou Decheng Biotechnology Co., LTD
- Amazewell — Guangzhou Decheng Biotechnology Co., LTD
- Amazewell — Guangzhou Decheng Biotechnology Co., LTD
- Amazewell — Guangzhou Decheng Biotechnology Co., LTD
- Amazewell — Guangzhou Decheng Biotechnology Co., LTD
- Amazewell — Guangzhou Decheng Biotechnology Co., LTD
- Amazewell — Guangzhou Decheng Biotechnology Co., LTD
Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Guangzhou Decheng Biotechnology Co., LTD
Sources (1)
- FDA UDI 61ef7139-d5be-4dd2-975b-d7b1a65b7b31 34 fields · synced Jun 6, 2026