Identity
- Trade Name
- Septal-H FDA UDI
- Generic Name
- Personal device holder, single-use FDA UDI
- Device Name
- Septal-H™ Premie size (1 Pack = 20 individual units) FDA UDI
- Model / Reference
- CP-5400 FDA UDI
- Description
- Septal-H™ Premie size (1 Pack = 20 individual units) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709078013119 FDA UDI
- FDA Product Code
- FMP FDA UDI
- GMDN Term
- Personal device holder, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6450 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
Yes
FDA UDI
Category: Personal device holder, single-use
Septal-H by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Westmed, Inc.
Sources (1)
- FDA UDI 4a6e7c92-780b-4665-9b20-2c393631c279 33 fields · synced May 29, 2026