Identity
- Trade Name
- ARIX Sternal System Bone Screw FDA UDI
- Generic Name
- Sternal fixation device FDA UDI
- Model / Reference
- 24L-SA-S19-TA FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800089434053 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Sternal fixation device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Sternal fixation device
ARIX Sternal System Bone Screw by Jeil Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sternal fixation device.
- STERNALOCK® BLU SYSTEM — BIOMET MICROFIXATION, INC · Class II
- Vanguard® — Biomet Orthopedics, Inc. · Class I
- SternaFuse® Fixation System — FUSION INNOVATIONS · Class II
- Valkyrie Thoracic Fixation System — J.M. Longyear Manufacturing, LLC · Class II
- STERNALOCK® BLU SYSTEM — BIOMET MICROFIXATION, INC · Class II
- Valkyrie Thoracic Fixation System — J.M. Longyear Manufacturing, LLC · Class II
- STERNALOCK® SYSTEM — BIOMET MICROFIXATION, INC · Class II
- Valkyrie Thoracic Fixation System — J.M. Longyear Manufacturing, LLC · Class II
Cleared under the same submission
K181806 also covers:
- ARIX Sternal System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
K221412 also covers:
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Rib System Bone Plate — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
- ARIX Sternal System Bone Screw — Jeil Medical Corporation
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
- Jeil Medical Corporation
Sources (1)
- FDA UDI 184aa3ea-3117-4552-8bd5-65c0a9b8c0a3 33 fields · synced Jun 1, 2026