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Responsive Respiratory

FDA UDI

Class I (US FDA UDI)

by Responsive Respiratory Inc.

Identity

Trade Name
Responsive Respiratory FDA UDI
Generic Name
Aerosol face mask, rebreathing, single-use FDA UDI
Device Name
Adult Aerosol Mask FDA UDI
Model / Reference
220-3510 FDA UDI
Description
Adult Aerosol Mask FDA UDI

Identifiers

Primary DI / UDI-DI
00851440007759 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Aerosol face mask, rebreathing, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Aerosol face mask, rebreathing, single-use

Responsive Respiratory by Responsive Respiratory Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Aerosol face mask, rebreathing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a50b29a1-89ef-4277-b333-9404839631a1 33 fields · synced Jun 1, 2026