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Multiroom IVF incubator MIRI

by Esco Medical Technologies Uab 2 variants

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 Number04779041940229 UDI-DI Date15 Jan 2026ListedStatusListed 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  • Withdrawn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
Multiroom IVF incubator
Generic Name
Assisted reproduction heater/incubator
Model / Reference
MIRI
Primary DI / UDI-DI
04779041940229
510(k) Number
FDA Product Code
MQG
GMDN Term
Assisted reproduction heater/incubator
Device Class
Class II
Regulation Number
884.6120
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K133742)

Other devices from Esco Medical Technologies Uab

See all devices from Esco Medical Technologies Uab →

Properties

  • Prescription Use
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • 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