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Vermed

FDA UDI

Class II (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
Vermed FDA UDI
Generic Name
Patient monitoring system module, electrocardiographic FDA UDI
Device Name
New NK 12 Pin CN to NK 6 Lead Patient Cable 3/6 Lea FDA UDI
Model / Reference
CBG-846600 FDA UDI
Description
New NK 12 Pin CN to NK 6 Lead Patient Cable 3/6 Lea FDA UDI

Identifiers

Catalog Number
CBG-846600 FDA UDI
Primary DI / UDI-DI
00009336004911 FDA UDI
510(k) Number
K992524 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Patient monitoring system module, electrocardiographic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Patient monitoring system module, electrocardiographic

Vermed by Graphic Controls Acquisition Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring system module, electrocardiographic.

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 6ce158f0-6adb-4d51-9f62-f6f0969ab35e 36 fields · synced Jun 1, 2026