Identity
- Trade Name
- Paeon Anterior Cervical Plate System FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- Implant Tray Base FDA UDI
- Model / Reference
- CP02-0009 FDA UDI
- Description
- Implant Tray Base FDA UDI
Identifiers
- Catalog Number
- CP02-0009 FDA UDI
- Primary DI / UDI-DI
- 00840273301455 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dry Heat Sterilization FDA UDI
Category: Instrument tray, reusable
Paeon Anterior Cervical Plate System by Aegis Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Instrument tray, reusable.
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- Hu-Friedy — Hu-Friedy Manufacturing Co., LLC · Class I
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- ASELTECH — Asel Tibbi Aletler A.S. · 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 |
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Manufacturer
- Manufacturer
- Aegis Spine, Inc.
Sources (1)
- FDA UDI 39ca7b71-ba07-4656-bcba-a9b4d0f4c25b 34 fields · synced Jun 1, 2026