Identity

Trade Name
CAM FDA UDI
Generic Name
Electrocardiograph, professional, single-channel FDA UDI
Device Name
CAM 14 FDA UDI
Model / Reference
14 FDA UDI
Description
CAM 14 FDA UDI

Identifiers

Primary DI / UDI-DI
00840682110075 FDA UDI
FDA Product Code
DQK FDA UDI
GMDN Term
Electrocardiograph, professional, single-channel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1425 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiograph, professional, single-channel

Cam by Ge Medical Systems Information Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiograph, professional, single-channel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 01184137-c9f6-4642-9e32-4474a7e80ed1 35 fields · synced Jun 8, 2026