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Prosidio P417R45

by Prosidio LLC

Prosidio P417R45 is a Class II device made by Prosidio LLC, listed in FDA GUDID since 5 Dec 2025 (UDI-DI 00850042909034), 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 Number00850042909034 UDI-DI Date5 Dec 2025ListedStatusListed 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  • Withdrawn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
Prosidio
Generic name
Rigid optical rhinolaryngoscope
Model / Ref / Catalog
P417R45
Primary DI / UDI-DI
00850042909034
FDA product code
EOB
GMDN term
Rigid optical rhinolaryngoscope
Device class
Class II
Regulation number
874.4760
GUDID distribution status
In Commercial Distribution
Sterilisation method
High-level Disinfectant

Similar devices

Other devices filed under FDA product code EOB (Nasopharyngoscope (Flexible Or Rigid)).

Other devices from Prosidio LLC

See all devices from Prosidio LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)