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Camco

FDA UDI

Class II (US FDA UDI)

by Cambridge Diagnostic Products, Inc.

Identity

Trade Name
Camco FDA UDI
Generic Name
Faecal occult blood IVD, reagent FDA UDI
Device Name
Positive control for guaiac based fecal occult blood slide tests FDA UDI
Model / Reference
700-C FDA UDI
Description
Positive control for guaiac based fecal occult blood slide tests FDA UDI

Identifiers

Catalog Number
700-C-1 FDA UDI
Primary DI / UDI-DI
00691573700154 FDA UDI
FDA Product Code
KHE FDA UDI
GMDN Term
Faecal occult blood IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6550 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

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

Dimensions & Sizes

Size
Total Volume — 7.5 Milliliter FDA UDI

Category: Faecal occult blood IVD, reagent

Camco by Cambridge Diagnostic Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Faecal occult blood IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cambridge Diagnostic Products, Inc.

Sources (1)

  • FDA UDI 2db054e3-28cf-4a99-96bc-23d913591ae5 37 fields · synced Jun 8, 2026