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Silicone cap BS2315-3

by Efer Endoscopy

Silicone cap BS2315-3 is a Class II device made by Efer Endoscopy, listed in FDA GUDID since 26 Oct 2023 (UDI-DI 03700620600075), 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 Number03700620600075 UDI-DI Date26 Oct 2023ListedStatusListed 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  • Withdrawn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
Silicone cap
Generic name
Rigid optical bronchoscope
Model / reference
BS2315-3
Primary DI / UDI-DI
03700620600075
FDA product code
EOQ
GMDN term
Rigid optical bronchoscope
Device class
Class II
Regulation number
874.4680
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Rigid optical bronchoscope

Similar devices

Other devices filed under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)).

Other devices from Efer Endoscopy

See all devices from Efer Endoscopy →

Properties

  • Sterilise before use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)