FDA UDI In Commercial Distribution 🇺🇸 United States

ARCADIUS XP C

DI: 04046955214686 · Model: ME520 · AESCULAP IMPLANT SYSTEMS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ARCADIUS XP C
Primary DI
04046955214686
Version / Model
ME520
Catalog Number
ME520
Company Name
AESCULAP IMPLANT SYSTEMS, LLC
Labeler DUNS
622600992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-14
Public Version
1
Public Version Date
2024-01-22
Public Version Status
New
Public Device Record Key
218f002f-3217-494b-b685-6c59ca53c8b3

Device Description

ARCADIUS XP C TRIAL./INSERTION TRAY TOP

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 04046955214686

Customer Contacts