Identity
- Trade Name
- Aero-Med FDA UDI
- Generic Name
- Cervical cytology brush FDA UDI
- Device Name
- Cytology Brushes FDA UDI
- Model / Reference
- 1010 FDA UDI
- Description
- Cytology Brushes FDA UDI
Identifiers
- Catalog Number
- 1010 FDA UDI
- Primary DI / UDI-DI
- 10810010891003 FDA UDI
- FDA Product Code
- HHT FDA UDI
- GMDN Term
- Cervical cytology brush 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
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
Category: Cervical cytology brush
Aero-Med by Aero-Med Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cervical cytology brush.
- Papette — Andwin Scientific · Class II
- Papette — CooperSurgical, Inc. · Class II
- Andwin Scientific — Andwin Scientific · Class II
- C60100 — B&B Company Co., Ltd. · Class II
- C60100 — B&B Company Co., Ltd. · Class II
- Andwin Scientific — Andwin Scientific · Class II
- SoftBiopsy — HISTOLOGICS LLC · Class I
- Papette — CooperSurgical, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Aero-Med Llc
Sources (1)
- FDA UDI 17179918-bf0d-4b4b-8996-cef526140229 34 fields · synced Jun 1, 2026