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Sperm Washing Medium

FDA UDI

Class II (US FDA UDI)

by Fujifilm Irvine Scientific, Inc.

Identity

Trade Name
Sperm Washing Medium FDA UDI
Generic Name
IVF medium FDA UDI
Device Name
Sperm Washing Medium- Made to order configuration FDA UDI
Model / Reference
9983-500mL FDA UDI
Description
Sperm Washing Medium- Made to order configuration FDA UDI

Identifiers

Catalog Number
9983 FDA UDI
Primary DI / UDI-DI
00857515006245 FDA UDI
FDA Product Code
MQL FDA UDI
GMDN Term
IVF medium FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6180 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 500 Milliliter FDA UDI

Category: IVF medium

Sperm Washing Medium by Fujifilm Irvine Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as IVF medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4fcdf6ed-f537-4af9-898c-072291f289d7 37 fields · synced May 30, 2026