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Amphetamine/Cocaine/Morphine Turnkey Split Cup

FDA UDI

Class II (US FDA UDI)

by Assure Tech. (hangzhou) Co., Ltd.

Identity

Trade Name
Amphetamine/Cocaine/Morphine Turnkey Split Cup FDA UDI
Generic Name
Opiate/opiate metabolite IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
1.0 FDA UDI

Identifiers

Primary DI / UDI-DI
06952804801441 FDA UDI
510(k) Number
K153465 FDA UDI
FDA Product Code
DIO FDA UDI
DJG FDA UDI
DKZ FDA UDI
GMDN Term
Opiate/opiate metabolite IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3250 FDA UDI
862.3650 FDA UDI
862.3100 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

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cocaine/cocaine metabolite IVD, kit, rapid ICT, clinicalOpiate/opiate metabolite IVD, kit, rapid ICT, clinicalAmphetamine-specific IVD, kit, rapid ICT, clinical

Amphetamine/Cocaine/Morphine Turnkey Split Cup by Assure Tech. (hangzhou) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Amphetamine-specific IVD, kit, rapid ICT, clinical.

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 93639d63-d6ce-4480-bc7d-a602224d19c0 33 fields · synced May 30, 2026