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Cholinesterase Gen.2

FDA UDI

Class I (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Cholinesterase Gen.2 FDA UDI
Generic Name
Cholinesterase dibucaine number (percentage inhibition) IVD, kit, spectrophotometry FDA UDI
Model / Reference
08105561190 FDA UDI

Identifiers

Catalog Number
08105561190 FDA UDI
Primary DI / UDI-DI
07613336133620 FDA UDI
FDA Product Code
DIH FDA UDI
GMDN Term
Cholinesterase dibucaine number (percentage inhibition) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.3240 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

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: Cholinesterase dibucaine number (percentage inhibition) IVD, kit, spectrophotometry

Cholinesterase Gen.2 by Roche Diagnostics Corp. — Class I — 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

Sources (1)

  • FDA UDI 7298c3f3-c44c-4a31-add4-758c63ef1dac 34 fields · synced May 30, 2026