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Salicyclate

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Salicyclate FDA UDI
Generic Name
Salicylate IVD, kit, enzyme spectrophotometry FDA UDI
Model / Reference
08058636190 FDA UDI

Identifiers

Catalog Number
08058636190 FDA UDI
Primary DI / UDI-DI
07613336121504 FDA UDI
510(k) Number
K954992 FDA UDI
FDA Product Code
DKJ FDA UDI
GMDN Term
Salicylate IVD, kit, enzyme spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3830 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: Salicylate IVD, kit, enzyme spectrophotometry

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

Similar devices

Also classified as Salicylate IVD, kit, enzyme spectrophotometry.

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 172bd301-7fd0-4724-af0a-6ed1b6ffc4ec 35 fields · synced May 30, 2026