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Fisherbrand

FDA UDI

Class I (US FDA UDI)

by Fisher Scientific Company L.l.c.

Identity

Trade Name
Fisherbrand FDA UDI
Generic Name
Cytological centrifuge funnel IVD FDA UDI
Device Name
DOUBLE CYTO FUNNEL WCARD 25PK FDA UDI
Model / Reference
10-356 FDA UDI
Description
DOUBLE CYTO FUNNEL WCARD 25PK FDA UDI

Identifiers

Catalog Number
10356 FDA UDI
Primary DI / UDI-DI
00613647022955 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cytological centrifuge funnel IVD

Fisherbrand by Fisher Scientific Company L.l.c. — 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

Sources (1)

  • FDA UDI 5dee74a3-bfba-4d5e-ba55-4fa162547ab1 35 fields · synced Jun 8, 2026