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Virginia National Guard

FDA UDI

Class II (US FDA UDI)

by Clinical Guard

Identity

Trade Name
Virginia National Guard FDA UDI
Generic Name
Pulse oximeter FDA UDI
Device Name
Contec CMS 50-DL Black Distributed by Clinical Guard FDA UDI
Model / Reference
50DL-B FDA UDI
Description
Contec CMS 50-DL Black Distributed by Clinical Guard FDA UDI

Identifiers

Catalog Number
Contec FDA UDI
Primary DI / UDI-DI
00851950008161 FDA UDI
510(k) Number
K082641 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
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

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

No

FDA UDI

Category: Pulse oximeter

Virginia National Guard by Clinical Guard — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Clinical Guard

Sources (1)

  • FDA UDI 85c86ec5-9fd3-4f21-8fa8-e09dd32466b2 35 fields · synced May 31, 2026