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Phencyclidine

FDA UDI

Class U (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Phencyclidine FDA UDI
Generic Name
Phencyclidine (PCP) IVD, kit, chemiluminescent immunoassay FDA UDI
Model / Reference
20738042122 FDA UDI

Identifiers

Catalog Number
20738042122 FDA UDI
Primary DI / UDI-DI
04015630993543 FDA UDI
510(k) Number
K951595 FDA UDI
FDA Product Code
LCM FDA UDI
GMDN Term
Phencyclidine (PCP) IVD, kit, chemiluminescent immunoassay 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

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Category: Phencyclidine (PCP) IVD, kit, chemiluminescent immunoassay

Phencyclidine by Roche Diagnostics Corp. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phencyclidine (PCP) IVD, kit, chemiluminescent immunoassay.

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 5d3383b4-f406-40fa-8ceb-2a0c72ffbcf2 35 fields · synced May 30, 2026