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Resp-O2 Non-Rebreather Elongated Mask, Adult, With Safety Vent, 7'(2.1m)

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Non-Rebreather Elongated Mask, Adult, With Safety Vent, 7'(2.1m) FDA UDI
Generic Name
Non-rebreathing oxygen face mask FDA UDI
Device Name
Crush- Resistant Tubing, 1000 mL Reservoir Bag, Universal Connector FDA UDI
Model / Reference
33050U FDA UDI
Description
Crush- Resistant Tubing, 1000 mL Reservoir Bag, Universal Connector FDA UDI

Identifiers

Primary DI / UDI-DI
00840117345225 FDA UDI
FDA Product Code
KGB FDA UDI
GMDN Term
Non-rebreathing oxygen face mask FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-rebreathing oxygen face mask

Resp-O2 Non-Rebreather Elongated Mask, Adult, With Safety Vent, 7'(2.1m) by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Non-rebreathing oxygen face mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 552767c1-3c67-47b1-8e4c-899e7411de7a 33 fields · synced Jun 1, 2026