FDA UDI In Commercial Distribution 🇺🇸 United States

SpermWash USA

DI: 08719747531730 · Model: SW-USA-0250 · Gynotec.B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SpermWash USA
Primary DI
08719747531730
Version / Model
SW-USA-0250
Company Name
Gynotec.B.V.
Labeler DUNS
489854382
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-15
Public Version
1
Public Version Date
2026-01-23
Public Version Status
New
Public Device Record Key
2d0a16be-3426-42a8-af1f-a613a9db9587

Device Description

SpermWash® USA is intended for in vitro procedures involving human gametes (sperm and oocytes), including washing of gametes, sperm swim-up procedures, intra-uterine insemination (IUI) of the spermatozoa and sperm injection during intracytoplasmic sperm injection (ICSI). SpermWash® USA can also be used for human embryo washing and holding, and for embryo transfer (ET) in the uterine cavity.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQL Media, Reproductive

GMDN Terms

Code Name
44046 IVF medium

Identifiers

Type ID
Package 08719747531747
Primary 08719747531730

Premarket Submissions

Submission Number Supplement Number
K242640 000

Device Sizes

Type Value Unit Text
Total Volume 250 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight