← Back to catalogue

Vit Kit - Warm NX

EUDAMEDFDA UDI

Class III (EU MDR)

Ref 90183

by Irvine Scientific, LLC.

Identity

Trade Name
Vit Kit - Warm NX EUDAMED
Vit Kit - Warm NX with Gentamicin and DSS FDA UDI
Generic Name
IVF medium FDA UDI
Device Name
Vit Kit - Warm NX EUDAMED
Vit Kit - Warm NX (Vitrification Kit for Warming) with Gentamicin and DSS. Includes 6x2mL Vials Thawing NX-TS (yellow cap), 2x1mL Vials Dilution NX-DS (orange cap) and 4x1mL Vials Washing NX-WS (red cap) FDA UDI
Model / Reference
90183 EUDAMEDFDA UDI
Description
Vit Kit - Warm NX (Vitrification Kit for Warming) with Gentamicin and DSS. Includes 6x2mL Vials Thawing NX-TS (yellow cap), 2x1mL Vials Dilution NX-DS (orange cap) and 4x1mL Vials Washing NX-WS (red cap) FDA UDI

Identifiers

Catalog Number
90183 FDA UDI
Primary DI / UDI-DI
00810195240293 EUDAMEDFDA UDI
Basic UDI-DI
B-00810195240293 EUDAMED
FDA Product Code
MQL FDA UDI
EMDN Code
U08020501 MATERIALS/SOLUTIONS FOR FREEZING/THAWING FOR ASSISTED REPRODUCTION EUDAMED
GMDN Term
IVF medium FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
884.6180 FDA UDI
Market of Registration
Netherlands EUDAMED
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

Yes

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Vit Kit - Warm NX by Irvine Scientific, Llc — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000007514
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (3)

  • EUDAMED 07bd88b2-1735-44b7-b613-cee0952a7b57 61 fields · synced Jul 30, 2026
  • FDA UDI 1b4af47f-d936-4f1a-b397-ca6b387528f7 35 fields · synced May 30, 2026
  • EUDAMED b269d249-e20f-4f9e-b282-285702ad9906 61 fields · synced Jul 30, 2026