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Ecstasy Panel Dip

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
Ecstasy Panel Dip FDA UDI
Generic Name
Amphetamine-specific IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
1.0 FDA UDI

Identifiers

Primary DI / UDI-DI
06952804801823 FDA UDI
510(k) Number
K170049 FDA UDI
FDA Product Code
NGG FDA UDI
GMDN Term
Amphetamine-specific IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3610 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

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: Amphetamine-specific IVD, kit, rapid ICT, clinical

Ecstasy Panel Dip 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 e472543d-38f7-4555-b679-85a791c8c217 33 fields · synced May 30, 2026