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RespVac™ RTG-02112

by Cutting Edge Hc Brands LLC

RespVac™ RTG-02112 is a Class I device made by Cutting Edge Hc Brands LLC, listed in FDA GUDID since 30 Dec 2022 (UDI-DI 00850108006240), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850108006240 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
RespVac™
Generic name
Secretion suction kit
Model / Ref / Catalog
RTG-02112
Description
RespVac Suction Catheter Kit Sterile 12FR
Primary DI / UDI-DI
00850108006240
FDA product code
BSY
GMDN term
Secretion suction kit
Device class
Class I
Regulation number
868.6810
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 12 French

Related devices

Category: Secretion suction kit

Similar devices in this category

Other devices filed under Secretion suction kit.

Other devices from Cutting Edge Hc Brands LLC

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)