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Responsive Respiratory, Inc.

FDA UDI

Class I (US FDA UDI)

by Responsive Respiratory Inc.

Identity

Trade Name
Responsive Respiratory, Inc. FDA UDI
Generic Name
Oxygen administration kit FDA UDI
Device Name
Yoke Washer - Brass with Viton Center 25/pack FDA UDI
Model / Reference
200-0120 FDA UDI
Description
Yoke Washer - Brass with Viton Center 25/pack FDA UDI

Identifiers

Primary DI / UDI-DI
00851440007476 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
Oxygen administration kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2700 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oxygen administration kit

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

Similar devices

Also classified as Oxygen administration kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 312d33cf-5714-434b-8cf2-bcf7cedde76b 33 fields · synced Jun 1, 2026