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ECO® II Cup

FDA UDI

Class II (US FDA UDI)

by W.h.p.m. Inc.

Identity

Trade Name
ECO® II Cup FDA UDI
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Device Name
DOA 6 in 1 Test ECO II Cup, 25Pcs/Box, CLIA Waived, BARB/BUP/BZO/MOR/MTD/OXY FDA UDI
Model / Reference
ECOII-7264 FDA UDI
Description
DOA 6 in 1 Test ECO II Cup, 25Pcs/Box, CLIA Waived, BARB/BUP/BZO/MOR/MTD/OXY FDA UDI

Identifiers

Catalog Number
ECOII-7264P FDA UDI
Primary DI / UDI-DI
00841824102026 FDA UDI
FDA Product Code
DJR FDA UDI
JXM FDA UDI
JXN FDA UDI
DJG FDA UDI
DIS FDA UDI
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3620 FDA UDI
862.3170 FDA UDI
862.3700 FDA UDI
862.3650 FDA UDI
862.3150 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

ECO® II Cup by W.h.p.m. Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple drugs of abuse IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W.h.p.m. Inc.

Sources (1)

  • FDA UDI 93997d7e-4bb1-413f-816d-8b5471c22ba4 34 fields · synced May 31, 2026