FDA UDI In Commercial Distribution 🇺🇸 United States

Paeon Anterior Cervical Plate System

DI: 00840273301622 · Model: CP02-0704 · Aegis Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Paeon Anterior Cervical Plate System
Primary DI
00840273301622
Version / Model
CP02-0704
Catalog Number
CP02-0704
Company Name
Aegis Spine, Inc.
Labeler DUNS
017993061
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-14
Public Version
3
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
b7bad0d5-96f0-4988-bcd3-448e3620b864

Device Description

Pin Holder

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Dry Heat Sterilization

Product Codes

Code Name
HXX Screwdriver

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00840273301622