Identity
- Trade Name
- Elation™ FDA UDI
- Generic Name
- Bronchial balloon catheter FDA UDI
- Model / Reference
- 00884450593837 FDA UDI
Identifiers
- Catalog Number
- P4L15/A FDA UDI
- Primary DI / UDI-DI
- 00884450593837 FDA UDI
- FDA Product Code
- KTI FDA UDI
- GMDN Term
- Bronchial balloon catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.4680 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bronchial balloon catheter
Elation™ by Merit Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bronchial balloon catheter.
- MultiStage® — Dongguan TT Medical, Inc. · Class II
- INSPIRA AIR — ACCLARENT, INC. · Class II
- MultiStage® — Dongguan TT Medical, Inc. · Class II
- UNIBLOCKER — Fuji Systems Corp. · Class II
- INSPIRA AIR — ACCLARENT, INC. · Class II
- Blowfish Micro-Infusion Catheter — Mercator MedSystems, Inc. · Class II
- INSPIRA AIR — ACCLARENT, INC. · Class II
- MultiStage® — Dongguan TT Medical, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Merit Medical Systems, Inc.
Sources (1)
- FDA UDI bcca9526-c971-42ad-9a22-3a856fc47b9c 34 fields · synced Jun 9, 2026