FDA UDI In Commercial Distribution 🇺🇸 United States

Cadence®

DI: 10381780417132 · Model: 10203102 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Cadence®
Primary DI
10381780417132
Version / Model
10203102
Catalog Number
10203102
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-29
Public Version
6
Public Version Date
2023-02-21
Public Version Status
Update
Public Device Record Key
5e592972-b281-400b-8ac5-5e22376b2f9c
Distribution End Date
2026-12-31

Device Description

45° Tibial Impactor Tip

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
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary 10381780417132
Previous 10381780356295

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.00in Lx 1.070in diameter