Identity
- Trade Name
- Quattro® FDA UDI
- Generic Name
- Bone lever/elevator, reusable FDA UDI
- Model / Reference
- CM-9008 FDA UDI
Identifiers
- Catalog Number
- CM-9008 FDA UDI
- Primary DI / UDI-DI
- M543CM9008 FDA UDI
- FDA Product Code
- NBH FDA UDI
- GMDN Term
- Bone lever/elevator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1100 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
Moist Heat or Steam Sterilization FDA UDI
Category: Bone lever/elevator, reusable
Quattro® by Cayenne Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone lever/elevator, reusable.
- Arthrex® — Arthrex, Inc. · Class I
- General Instruments — ALPHATEC SPINE, INC. · Class I
- IdentiTi — ALPHATEC SPINE, INC. · Class I
- Intervertebral Disc Preparation Instruments — ALPHATEC SPINE, INC. · Class I
- HAT-TRICK — Smith & Nephew, Inc. · Class I
- ORTHOMED — ORTHO-MED, INC. · Class I
- Symmetry Allerdyce — SYMMETRY SURGICAL INC. · Class I
- Life Instruments — Life Instrument Corporation · 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
- Cayenne Medical, Inc.
Sources (1)
- FDA UDI 75c81198-dc39-453f-b025-5dc0c1942e2c 33 fields · synced Jun 1, 2026