← Back to catalogue

ISolate® Stock Solution

FDA UDI

Class II (US FDA UDI)

by Fujifilm Irvine Scientific, Inc.

Identity

Trade Name
ISolate® Stock Solution FDA UDI
Generic Name
IVF medium FDA UDI
Device Name
ISolate® Stock Solution FDA UDI
Model / Reference
99275-500ML FDA UDI
Description
ISolate® Stock Solution FDA UDI

Identifiers

Catalog Number
99275 FDA UDI
Primary DI / UDI-DI
00857515006016 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
Not 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 500 Milliliter FDA UDI

ISolate® Stock Solution by Fujifilm Irvine Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 40dd0210-da3b-4358-8022-d57784df8b13 38 fields · synced Jun 8, 2026