Identity
- Trade Name
- RELIEVA LUMA FDA UDI
- Generic Name
- Paranasal sinus-illumination light guide cable FDA UDI
- Device Name
- RELIEVA LUMA LIGHT GUIDE CABLE ADAPTER - STORZ FDA UDI
- Model / Reference
- SISLGCASTORZ FDA UDI
- Description
- RELIEVA LUMA LIGHT GUIDE CABLE ADAPTER - STORZ FDA UDI
Identifiers
- Catalog Number
- SISLGCASTORZ FDA UDI
- Primary DI / UDI-DI
- 10705031205895 FDA UDI
- FDA Product Code
- EQH FDA UDI
- GMDN Term
- Paranasal sinus-illumination light guide cable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4350 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
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: Paranasal sinus-illumination light guide cable
Relieva Luma by Acclarent, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Paranasal sinus-illumination light guide cable.
- RELIEVA LUMA SENTRY — ACCLARENT, INC. · Class I
- RELIEVA LUMA — ACCLARENT, INC. · Class I
- RELIEVA LUMA — ACCLARENT, INC. · Class I
- RELIEVA LUMA SENTRY — ACCLARENT, INC. · Class I
- RELIEVA LUMA — ACCLARENT, INC. · Class I
- RELIEVA LUMA — ACCLARENT, INC. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Acclarent, Inc.
Sources (1)
- FDA UDI 6cbac395-34ff-4dcc-a0a6-0751b051af03 36 fields · synced May 30, 2026