FDA UDI Not in Commercial Distribution 🇺🇸 United States

ARCADIUS

DI: 04046955091089 · Model: ME976P · AESCULAP IMPLANT SYSTEMS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ARCADIUS
Primary DI
04046955091089
Version / Model
ME976P
Catalog Number
ME976P
Company Name
AESCULAP IMPLANT SYSTEMS, LLC
Labeler DUNS
622600992
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-30
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
17fd13dd-9100-4874-9036-ba1c35f16ccc
Distribution End Date
2021-05-13

Device Description

ARCADIUS PUSHING BLOCK 10/6

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 04046955091089

Customer Contacts