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Cholinesterase

FDA UDI

Class I (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Cholinesterase FDA UDI
Generic Name
Acetylcholinesterase IVD, kit, spectrophotometry FDA UDI
Model / Reference
11877763216 FDA UDI

Identifiers

Catalog Number
11877763216 FDA UDI
Primary DI / UDI-DI
04015630991549 FDA UDI
FDA Product Code
DIH FDA UDI
GMDN Term
Acetylcholinesterase 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

No

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: Acetylcholinesterase IVD, kit, spectrophotometry

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

Similar devices

Also classified as Acetylcholinesterase IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0a202f0b-403b-49ce-955c-2cd5e8e55468 33 fields · synced Jun 8, 2026