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TOX/See

FDA UDI

Class U (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
TOX/See FDA UDI
Generic Name
Phencyclidine (PCP) IVD, kit, rapid ICT, clinical FDA UDI
Device Name
TOX/See Drug Screen Test PCP FDA UDI
Model / Reference
194-5194 FDA UDI
Description
TOX/See Drug Screen Test PCP FDA UDI

Identifiers

Catalog Number
1945194 FDA UDI
Primary DI / UDI-DI
00847817000683 FDA UDI
FDA Product Code
LCM FDA UDI
GMDN Term
Phencyclidine (PCP) 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

Yes

FDA UDI

Category: Phencyclidine (PCP) IVD, kit, rapid ICT, clinical

TOX/See by Bio-Rad Laboratories — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phencyclidine (PCP) IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb459cbd-ce73-4370-9fb1-9fb0d4814f1d 36 fields · synced Jun 8, 2026