Identity
- Trade Name
- Cytology Brush FDA UDI
- Generic Name
- Flexible endoscopic cytology brush, single-use FDA UDI
- Device Name
- Flexible endoscopic cytology brush FDA UDI
- Model / Reference
- CB-1315 FDA UDI
- Description
- Flexible endoscopic cytology brush FDA UDI
Identifiers
- Catalog Number
- CB-1315 FDA UDI
- Primary DI / UDI-DI
- 00816207020525 FDA UDI
- 510(k) Number
- K800966 FDA UDI
- FDA Product Code
- FDX FDA UDI
- GMDN Term
- Flexible endoscopic cytology brush, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 1.7 Millimeter FDA UDILength — 150 Centimeter FDA UDI
Cytology Brush by Endo-Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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 II | Pending data |
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Manufacturer
- Manufacturer
- Endo-Therapeutics, Inc.
Sources (1)
- FDA UDI bf49c17a-8f8b-40cc-9719-adb9b963e01e 39 fields · synced May 30, 2026