Identity
- Trade Name
- Hetaida 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
- 06970289035724 FDA UDI
- 510(k) Number
- K241202 FDA UDI
- FDA Product Code
- BTA FDA UDI
- GMDN Term
- Nasal aspirator, electric FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4780 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
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: Nasal aspirator, electric
Hetaida by Hetaida Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasal aspirator, electric.
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- Nasal aspirator — Shenzhen Dongjiang Technology Co., Ltd. · Class II
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- GROWNSY — Oak Tech LLC · Class II
Cleared under the same submission
K241202 also covers:
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 54c73cfd-5bbf-4619-9db5-13b5da3432d9 36 fields · synced May 29, 2026