Identity
- Trade Name
- Nasopore FDA UDI
- Generic Name
- Intranasal splint, biodegradable FDA UDI
- Device Name
- Standard 4cm FDA UDI
- Model / Reference
- 5400212004s FDA UDI
- Description
- Standard 4cm FDA UDI
Identifiers
- Catalog Number
- 5400-212-004S FDA UDI
- Primary DI / UDI-DI
- 07613327500387 FDA UDI
- FDA Product Code
- LYA FDA UDI
- GMDN Term
- Intranasal splint, biodegradable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4780 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Intranasal splint, biodegradable
Nasopore by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Husteon MeshNasal — MediFab Co., Ltd · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 7450c58f-93cb-4c81-bfa9-46d86bc29f62 36 fields · synced Jun 8, 2026