FDA UDI In Commercial Distribution 🇺🇸 United States

Paeon Posterior Cervical Fixation System

DI: 00840273311065 · Model: CS02-0712 · Aegis Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Paeon Posterior Cervical Fixation System
Primary DI
00840273311065
Version / Model
CS02-0712
Catalog Number
CS02-0712
Company Name
Aegis Spine, Inc.
Labeler DUNS
017993061
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-03
Public Version
1
Public Version Date
2022-05-11
Public Version Status
New
Public Device Record Key
80e6453a-49bc-4256-bb42-2b374038cfd7

Device Description

REDUCTION CUTTER

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44805 Orthopaedic implantable-device cutter

Identifiers

Type ID
Primary 00840273311065