← Back to catalogue

Thawing Media

FDA UDI

Class II (US FDA UDI)

by Kitazato Corporation

Identity

Trade Name
Thawing Media FDA UDI
Generic Name
IVF medium kit FDA UDI
Device Name
Contains TS×2,DS and WS FDA UDI
Model / Reference
VT602US FDA UDI
Description
Contains TS×2,DS and WS FDA UDI

Identifiers

Primary DI / UDI-DI
14582231462602 FDA UDI
FDA Product Code
MQL FDA UDI
GMDN Term
IVF medium kit 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

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: IVF medium kit

Thawing Media by Kitazato Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as IVF medium kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 458b9b18-cb0e-415d-a31e-14e762364709 34 fields · synced May 30, 2026