Identity
- Trade Name
- Double Cytology Funnel w/ White Card and Caps FDA UDI
- Generic Name
- Cytological centrifuge funnel IVD FDA UDI
- Model / Reference
- BMP-CYTO-DB25 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00853778007005 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
Double Cytology Funnel w/ White Card and Caps by Biomedical Polymers, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cytological centrifuge funnel IVD.
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- Cytopro Magnum Sample Chambers w/ caps — ELITECHGROUP INC. · Class I
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Biomedical Polymers, Inc.
Sources (1)
- FDA UDI cc2e74e2-5c83-402a-b679-85185186aba7 32 fields · synced May 30, 2026