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Preferred Med Supply

FDA UDI

Class II (US FDA UDI)

by Deus Vult, Llc

Identity

Trade Name
Preferred Med Supply FDA UDI
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Multi-panel Drug Test Cup FDA UDI
Model / Reference
PF12P FDA UDI
Description
Multi-panel Drug Test Cup FDA UDI

Identifiers

Catalog Number
PF12P FDA UDI
Primary DI / UDI-DI
00860004081609 FDA UDI
510(k) Number
K182654 FDA UDI
FDA Product Code
QBF FDA UDI
NFY FDA UDI
NGI FDA UDI
NGL FDA UDI
PTG FDA UDI
NGG FDA UDI
NGM FDA UDI
PTH FDA UDI
QAW FDA UDI
NFT FDA UDI
NFW FDA UDI
NFV FDA UDI
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3700 FDA UDI
862.3250 FDA UDI
862.3640 FDA UDI
862.3650 FDA UDI
862.3620 FDA UDI
862.3610 FDA UDI
862.3150 FDA UDI
862.3910 FDA UDI
862.3100 FDA UDI
862.3870 FDA UDI
862.3170 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Preferred Med Supply by Deus Vult, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Deus Vult, Llc

Sources (1)

  • FDA UDI 3ad277b5-1210-4531-8f4c-bd6f5162fedf 37 fields · synced May 30, 2026