← Back to catalogue

RespVent™

FDA UDI

Class I (US FDA UDI)

by Cutting Edge Hc Brands Llc

Identity

Trade Name
RespVent™ FDA UDI
Generic Name
Straight/elbow breathing circuit connector, single-use FDA UDI
Device Name
RespVent Closed Suction System T-Piece Tracheostomy Adult w/MDI Adapter 14F ADULT FDA UDI
Model / Reference
RTG-02300 FDA UDI
Description
RespVent Closed Suction System T-Piece Tracheostomy Adult w/MDI Adapter 14F ADULT FDA UDI

Identifiers

Catalog Number
RTG-02300 FDA UDI
Primary DI / UDI-DI
00850108006356 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Straight/elbow breathing circuit connector, single-use 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

Yes

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

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 14 French FDA UDI
Length — 30.5 Centimeter FDA UDI

Category: Straight/elbow breathing circuit connector, single-use

RespVent™ by Cutting Edge Hc Brands Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Straight/elbow breathing circuit connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cutting Edge Hc Brands Llc

Sources (1)

  • FDA UDI 09e18a03-8ce5-438f-aaf5-410fe64bd72c 36 fields · synced May 30, 2026