Identity
- Trade Name
- At Home Drug Test for Marijuana FDA UDI
- Generic Name
- Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- Urine based drug of abuse test for THC FDA UDI
- Model / Reference
- 9078T FDA UDI
- Description
- Urine based drug of abuse test for THC FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00674033090781 FDA UDI
- FDA Product Code
- MVO FDA UDI
- GMDN Term
- Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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: Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical
At Home Drug Test for Marijuana by Phamatech, Incorporated — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical.
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- Welcheck Marijuana(THC) Urine Test Dipcard — Safecare Biotech (Hangzhou) Co., Ltd. · Class II
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 U | Pending data |
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Manufacturer
- Manufacturer
- Phamatech, Incorporated
Sources (1)
- FDA UDI 647277fe-fcb7-4ac3-bdc5-c70c523043ad 35 fields · synced Jun 8, 2026