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Prosidio P317R30

by Prosidio LLC

Prosidio P317R30 is a Class II device made by Prosidio LLC, listed in FDA GUDID since 24 Oct 2026 (UDI-DI 00860006918774), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860006918774 UDI-DI Date24 Oct 2026ListedStatusListed 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  • Withdrawn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
P317R30
Primary DI / UDI-DI
00860006918774
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
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)