The DivaCup Model A PL

by Diva International Inc 3 variants

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00050428088852 UDI-DI	Date31 Mar 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: The DivaCup
Generic Name: Menstrual cup/disc, non-latex, reusable
Model / Ref / Catalog: Model A PL, 722537

Primary DI / UDI-DI: 00050428088852
FDA Product Code: HHE
GMDN Term: Menstrual cup/disc, non-latex, reusable

Device Class: Class II
Regulation Number: 884.5400
GUDID distribution status: In Commercial Distribution

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Properties

Premarket Exempt
Lot / Batch Number
Manufacturing Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No