Identity
- Trade Name
- Cytology Brush FDA UDI
- Generic Name
- Cervical cytology scraper, single-use FDA UDI
- Device Name
- 8" Cytology Brush FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 8" Cytology Brush FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00813360023011 FDA UDI
- FDA Product Code
- HHT FDA UDI
- GMDN Term
- Cervical cytology scraper, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4530 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cervical cytology scraper, single-use
Cytology Brush by Team Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cervical cytology scraper, single-use.
- ViaMed — RECE INTERNATIONAL CORP. · Class II
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- SpiraBrush CX — HISTOLOGICS LLC · Class I
- Safetex — Andwin Scientific · Class II
- Spatula — CooperSurgical, Inc. · Class II
- 6.5" Cytology Brush — TEAM TECHNOLOGIES, INC. · Class II
- Cytology Brush — TEAM TECHNOLOGIES, INC. · Class II
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
- Team Technologies, Inc.
Sources (1)
- FDA UDI 4e5ad2fc-9e3d-4d8d-87d0-d4b97f59fb70 33 fields · synced May 30, 2026