Identity
- Trade Name
- YOOKO FDA UDI
- Generic Name
- Nasal aspirator, electric FDA UDI
- Device Name
- Electric Nasal Aspirator FDA UDI
- Model / Reference
- HTD2601US FDA UDI
- Description
- Electric Nasal Aspirator FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970289035366 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Nasal aspirator, electric FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Nasal aspirator, electric
Yooko by Hetaida Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- GROWNSY — Oak Tech LLC · 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
- Hetaida Technology Co., Ltd
Sources (1)
- FDA UDI 96bb3fca-3c38-466d-bcaf-df68f1eee65e 35 fields · synced May 30, 2026