Identity
- Trade Name
- Arthrex® FDA UDI
- Generic Name
- Bone grafting cannula FDA UDI
- Device Name
- Bio Delivery Cannula - Trochanteric Nail FDA UDI
- Model / Reference
- ABS-1094 FDA UDI
- Description
- Bio Delivery Cannula - Trochanteric Nail FDA UDI
Identifiers
- Catalog Number
- ABS-1094 FDA UDI
- Primary DI / UDI-DI
- 00888867455870 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Bone grafting cannula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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: Bone grafting cannula
Arthrex® by Arthrex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone grafting cannula.
- Bongold Bone Graft Material — Beijing Allgens Medical Science & Technology Co., Ltd. · Class II
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- One-Shot — Shanghai Kinetic Medical Co., Ltd. · Class I
- Vital™ — BIOMET SPINE LLC · Class I
- Precision Cannula — Zimmer, Inc. · Class I
- Bongold Bone Graft Material — Beijing Allgens Medical Science & Technology Co., Ltd. · 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 I | Pending data |
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Manufacturer
- Manufacturer
- Arthrex, Inc.
Sources (1)
- FDA UDI 07cdec1b-395b-4956-aafa-8e026d90ada3 35 fields · synced Jun 8, 2026