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Esotest Multi Monitor 30115

by Fiab SpA

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08054953344003 UDI-DI Date6 Dec 2019ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Esotest Multi Monitor
Generic Name
Oesophageal temperature monitor
Model / Ref / Catalog
30115
Primary DI / UDI-DI
08054953344003
510(k) Number
FDA Product Code
FLL
GMDN Term
Oesophageal temperature monitor
Device Class
Class II
Regulation Number
880.2910
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: Oesophageal temperature monitor

Cleared under the same submission (K192210)

Similar devices

Also classified as Oesophageal temperature monitor.

Other devices from Fiab SpA

See all devices from Fiab SpA →

Properties

  • Prescription Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No