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MicroCell

FDA UDI

Class I (US FDA UDI)

by Vitrolife AB

Identity

Trade Name
MicroCell FDA UDI
Generic Name
General specimen microscopy slide IVD, single-use FDA UDI
Device Name
MicroCell, 20um, 4-Chamber FDA UDI
Model / Reference
15424 FDA UDI
Description
MicroCell, 20um, 4-Chamber FDA UDI

Identifiers

Primary DI / UDI-DI
10805360018033 FDA UDI
FDA Product Code
GHO FDA UDI
GMDN Term
General specimen microscopy slide IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen microscopy slide IVD, single-use

MicroCell by Vitrolife AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen microscopy slide IVD, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vitrolife AB

Sources (1)

  • FDA UDI e17f8573-fc1f-46c2-a470-1a078b21b332 33 fields · synced May 30, 2026