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PherDal At-Home Insemination Kit

by Pherdal Fertility Science, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00860011225126 UDI-DI Date6 Jul 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Home-use artificial insemination kit
Model / Reference
PherDal
Primary DI / UDI-DI
00860011225126
510(k) Number
FDA Product Code
QYZ
GMDN Term
Home-use artificial insemination kit
Device Class
Class II
Regulation Number
884.6110
GUDID distribution status
In Commercial Distribution
Sterilization Method
Radiation Sterilization

Other devices from Pherdal Fertility Science, Inc.

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Manufacturing Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No