Identity
- Trade Name
- Snorkel FDA UDI
- Generic Name
- General-purpose suction system, line-powered FDA UDI
- Model / Reference
- 10812594010382 FDA UDI
Identifiers
- Catalog Number
- N275 FDA UDI
- Primary DI / UDI-DI
- 10812594010382 FDA UDI
- FDA Product Code
- JOL FDA UDI
- GMDN Term
- General-purpose suction system, line-powered 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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General-purpose suction system, line-powered
Snorkel by Neotech Products LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Winx® — Apnicure, Inc. · Class II
- Winx® — Apnicure, 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
- Neotech Products LLC
Sources (1)
- FDA UDI ab4094ae-d7c7-4765-b9ab-b5782c50a6ce 33 fields · synced May 30, 2026