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Resp-O2 Universal Suction Tubing Kit

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Resp-O2 Universal Suction Tubing Kit FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
CONTENTS: 1/4" x 6" Suction Tube, Soft Elbow, Rigid Elbow, Hydrophobic Disc, 16" Silicone Tube (cut to size) FDA UDI
Model / Reference
32410 FDA UDI
Description
CONTENTS: 1/4" x 6" Suction Tube, Soft Elbow, Rigid Elbow, Hydrophobic Disc, 16" Silicone Tube (cut to size) FDA UDI

Identifiers

Primary DI / UDI-DI
00840117338647 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

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: Suction/irrigation tubing, single-use

Resp-O2 Universal Suction Tubing Kit by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 5f0bcb29-eb96-45ba-a5b2-570932230f64 33 fields · synced May 31, 2026