← Back to catalogue

Single Cytology Funnel w/ Brown Card

FDA UDI

Class I (US FDA UDI)

by Biomedical Polymers, Inc.

Identity

Trade Name
Single Cytology Funnel w/ Brown Card FDA UDI
Generic Name
Cytological centrifuge funnel IVD FDA UDI
Model / Reference
BMP-CYTO-S50BP FDA UDI

Identifiers

Primary DI / UDI-DI
00853778007142 FDA UDI
FDA Product Code
KET FDA UDI
GMDN Term
Cytological centrifuge funnel IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cytological centrifuge funnel IVD

Single Cytology Funnel w/ Brown Card by Biomedical Polymers, 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

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

Manufacturer

Sources (1)

  • FDA UDI e745cc52-f049-484c-bdbd-3d4012bfba18 32 fields · synced Jun 8, 2026