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Resp-O2 Closed Suction Tracheostomy Catheters, Sterile

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Closed Suction Tracheostomy Catheters, Sterile FDA UDI
Generic Name
Closed-suction breathing circuit connector/switch FDA UDI
Device Name
Adult, Double Swivel Elbow(DSE), Diameter (4.6mm (14FR), Length ( Tracheostomy 30.5cm /12in ). CONTENTS: Catheter, MDI Port, 15mm x 22 mm Flex Tube, Change of Day. FDA UDI
Model / Reference
31012 FDA UDI
Description
Adult, Double Swivel Elbow(DSE), Diameter (4.6mm (14FR), Length ( Tracheostomy 30.5cm /12in ). CONTENTS: Catheter, MDI Port, 15mm x 22 mm Flex Tube, Change of Day. FDA UDI

Identifiers

Primary DI / UDI-DI
00840117305755 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Closed-suction breathing circuit connector/switch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 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

No

FDA UDI

Category: Closed-suction breathing circuit connector/switch

Resp-O2 Closed Suction Tracheostomy Catheters, Sterile by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-suction breathing circuit connector/switch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 3c432539-c6c8-43e1-bbb0-f8fd1d1c21ce 33 fields · synced May 30, 2026