← Back to catalogue

Vermed

FDA UDI

Class II (US FDA UDI)

by Graphic Controls Acquisition Corp

Identity

Trade Name
Vermed FDA UDI
Generic Name
Pulse oximetry telemetric monitoring system FDA UDI
Device Name
NK to NK Cable FDA UDI
Model / Reference
CBG-A400-900P FDA UDI
Description
NK to NK Cable FDA UDI

Identifiers

Catalog Number
CBG-A400-900P FDA UDI
Primary DI / UDI-DI
00009336006229 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximetry telemetric monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 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: Pulse oximetry telemetric monitoring system

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

Similar devices

Also classified as Pulse oximetry telemetric monitoring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Graphic Controls Acquisition Corp

Sources (1)

  • FDA UDI ee4d2e81-ffe0-46a8-9117-0dc7e37a1b8b 35 fields · synced May 30, 2026