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Nidacon

FDA UDI

Class II (US FDA UDI)

by Nidacon International AB

Identity

Trade Name
Nidacon FDA UDI
Generic Name
Spermatozoa/semen motility medium supplement FDA UDI
Device Name
The product is intended for use as an oil overlay during gamete and embryo culture for ART, (Assisted Reproduction Technology) and during manipulations outside the incubator. FDA UDI
Model / Reference
NidOil™ FDA UDI
Description
The product is intended for use as an oil overlay during gamete and embryo culture for ART, (Assisted Reproduction Technology) and during manipulations outside the incubator. FDA UDI

Identifiers

Catalog Number
NO-300 FDA UDI
Primary DI / UDI-DI
07350025610184 FDA UDI
510(k) Number
K012123 FDA UDI
FDA Product Code
MQL FDA UDI
GMDN Term
Spermatozoa/semen motility medium supplement 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Spermatozoa/semen motility medium supplement

Nidacon by Nidacon International AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spermatozoa/semen motility medium supplement.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 44f332bd-310f-4bbc-b4e9-c45dc61b0e0a 37 fields · synced May 30, 2026