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YO Home Sperm Test

FDA UDI

by M.e.s. Medical Electronic Systems Ltd.

Identity

Trade Name
YO Home Sperm Test FDA UDI
Generic Name
Motile sperm concentration IVD, kit, imaging, self-testing FDA UDI
Model / Reference
For Galaxy 6 FDA UDI

Identifiers

Primary DI / UDI-DI
07290016650075 FDA UDI
GMDN Term
Motile sperm concentration IVD, kit, imaging, self-testing FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Motile sperm concentration IVD, kit, imaging, self-testing

YO Home Sperm Test by M.e.s. Medical Electronic Systems Ltd. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Motile sperm concentration IVD, kit, imaging, self-testing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
M.e.s. Medical Electronic Systems Ltd.

Sources (1)

  • FDA UDI 38d37463-5de5-44d4-85f7-e5d9713dfbf4 32 fields · synced May 30, 2026