← Back to catalogue

Immunalysis

FDA UDI

Class I (US FDA UDI)

by Immunalysis Corporation

Identity

Trade Name
Immunalysis FDA UDI
Generic Name
Buprenorphine IVD, control FDA UDI
Device Name
Buprenorphine Urine Control Set FDA UDI
Model / Reference
04W30-10 FDA UDI
Description
Buprenorphine Urine Control Set FDA UDI

Identifiers

Catalog Number
04W30-10 FDA UDI
Primary DI / UDI-DI
00840937111192 FDA UDI
FDA Product Code
LAS FDA UDI
GMDN Term
Buprenorphine IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3280 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

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: Buprenorphine IVD, control

Immunalysis by Immunalysis Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Buprenorphine IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0243c87b-543d-4524-8ee8-fb742f3b0fa2 35 fields · synced May 30, 2026