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Cytopro Magnum Sample Chambers w/ caps

FDA UDI

Class I (US FDA UDI)

by Elitechgroup Inc.

Identity

Trade Name
Cytopro Magnum Sample Chambers w/ caps FDA UDI
Generic Name
Cytological centrifuge funnel IVD FDA UDI
Device Name
Cytopro Magnum Sample Chambers w/ caps FDA UDI
Model / Reference
SS-234 FDA UDI
Description
Cytopro Magnum Sample Chambers w/ caps FDA UDI

Identifiers

Catalog Number
SS-234 FDA UDI
Primary DI / UDI-DI
03661540303272 FDA UDI
FDA Product Code
IFB FDA UDI
GMDN Term
Cytological centrifuge funnel IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

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: Cytological centrifuge funnel IVD

Cytopro Magnum Sample Chambers w/ caps by Elitechgroup Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cytological centrifuge funnel IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elitechgroup Inc.

Sources (1)

  • FDA UDI 03651d15-b3e4-4b61-82e8-7defc06a952f 35 fields · synced Jun 6, 2026