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Durex Intense 00302340996136

by Reckitt Benckiser LLC

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 Number00302340996136 UDI-DI Date2 Mar 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  • Withdrawn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
Durex Intense
Generic Name
Basic male condom, synthetic polymer
Model / Reference
00302340996136
Primary DI / UDI-DI
00302340996136
510(k) Number
FDA Product Code
MOL
GMDN Term
Basic male condom, synthetic polymer
Device Class
Class II
Regulation Number
884.5300
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K240896)

Other devices from Reckitt Benckiser LLC

See all devices from Reckitt Benckiser LLC →

Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (11)

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