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I-Gel®, Supraglottic Airway, Size 2.0, Small Paediatric, 10-25kg (Us) 8202030

by Intersurgical Incorporated

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05030267169894 UDI-DI Date2 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
I-Gel®, Supraglottic Airway, Size 2.0, Small Paediatric, 10-25kg (Us)
Generic Name
Laryngeal mask airway, single-use
Model / Reference
8202030
Primary DI / UDI-DI
05030267169894
FDA Product Code
CAE
GMDN Term
Laryngeal mask airway, single-use
Device Class
Class I
Regulation Number
868.5110
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Other devices from Intersurgical Incorporated

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (6)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Serial Number: No