Skip to content

CaseBioscience® WHMO-100

by Casebioscience, Inc.

CaseBioscience® WHMO-100 is a Class II device made by Casebioscience, Inc., listed in FDA GUDID since 30 Oct 2025 (UDI-DI 07540161790066), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07540161790066 UDI-DI Date30 Oct 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
CaseBioscience®
Generic name
IVF medium
Model / Ref / Catalog
WHMO-100
Primary DI / UDI-DI
07540161790066
FDA product code
MQL
GMDN term
IVF medium
Device class
Class II
Regulation number
884.6180
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 100 Milliliter

Similar devices

Other devices filed under FDA product code MQL (Media, Reproductive).

Other devices from Casebioscience, Inc.

See all devices from Casebioscience, Inc. →

Properties

  • Supplied sterile
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)