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BPR Medical

FDA UDI

Class II (US FDA UDI)

by Bpr Medical, Ltd.

Identity

Trade Name
BPR Medical FDA UDI
Generic Name
Demand valve FDA UDI
Device Name
Oxygen demand valve. Used for the self-administration of oxygen by a spontaneously breathing patient. FDA UDI
Model / Reference
Oxygen demand valve 3m hose DISS FDA UDI
Description
Oxygen demand valve. Used for the self-administration of oxygen by a spontaneously breathing patient. FDA UDI

Identifiers

Catalog Number
831-5003 FDA UDI
Primary DI / UDI-DI
05060274500687 FDA UDI
510(k) Number
K082345 FDA UDI
FDA Product Code
CBP FDA UDI
GMDN Term
Demand valve FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5870 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: Demand valve

BPR Medical by Bpr Medical, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Demand valve.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bpr Medical, Ltd.

Sources (1)

  • FDA UDI 41873b55-66f7-42b6-a2b2-37821be33a14 36 fields · synced May 29, 2026