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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
Telemetric pulse oximeter FDA UDI
Device Name
Philips compatible Large Soft Tip Sp02 Sensor,8-Pin FDA UDI
Model / Reference
PRG-A900-1006V FDA UDI
Description
Philips compatible Large Soft Tip Sp02 Sensor,8-Pin FDA UDI

Identifiers

Catalog Number
PRG-A900-1006V FDA UDI
Primary DI / UDI-DI
00009336006281 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Telemetric pulse oximeter 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: Telemetric pulse oximeter

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

Similar devices

Also classified as Telemetric pulse oximeter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Graphic Controls Acquisition Corp

Sources (1)

  • FDA UDI e17a88e0-32d3-4acf-ab3b-f8477085a2d4 35 fields · synced May 30, 2026