Identity
- Trade Name
- Muc-Away, Comfort Soft FDA UDI
- Generic Name
- Nasal aspirator, manual FDA UDI
- Device Name
- Nasal Aspiration Device, 3.25" FDA UDI
- Model / Reference
- 0490 FDA UDI
- Description
- Nasal Aspiration Device, 3.25" FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709078004681 FDA UDI
- FDA Product Code
- GCX FDA UDI
- GMDN Term
- Nasal aspirator, manual 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
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
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, manual
Muc-Away, Comfort Soft by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Safety 1st — DOREL JUVENILE GROUP, INC. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
- Dr. Brown's — Dr. Brown's Company · Class I
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
- Westmed, Inc.
Sources (1)
- FDA UDI dcff8907-e327-4633-ad5a-54ff93c66965 33 fields · synced May 31, 2026