← Back to catalogue

ES(Equilibration Solution) Pack 4 vials

FDA UDI

Class II (US FDA UDI)

by Kitazato Corporation

Identity

Trade Name
ES(Equilibration Solution) Pack 4 vials FDA UDI
Generic Name
IVF medium kit FDA UDI
Device Name
ES(Equilibration Solution) Pack 4x1.5ml vials FDA UDI
Model / Reference
VT601US-ESx4 FDA UDI
Description
ES(Equilibration Solution) Pack 4x1.5ml vials FDA UDI

Identifiers

Catalog Number
91239 FDA UDI
Primary DI / UDI-DI
14573316386173 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: IVF medium kit

ES(Equilibration Solution) Pack 4 vials 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 63e70f16-f297-48ec-9b39-410fbf4f574d 34 fields · synced Jun 1, 2026