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SunMed 9-0204-10

by SunMed

SunMed 9-0204-10 is a Class I device made by SunMed, listed in FDA GUDID since 12 Mar 2024 (UDI-DI 10889483007082), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10889483007082 UDI-DI Date12 Mar 2024ListedStatusListed 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  • Withdrawn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
SunMed
Generic name
Endotracheal tube holder
Model / Ref / Catalog
9-0204-10
Primary DI / UDI-DI
10889483007082
FDA product code
BSR
GMDN term
Endotracheal tube holder
Device class
Class I
Regulation number
868.5790
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endotracheal tube holder

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Other devices filed under Endotracheal tube holder.

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Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)