FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780511243 · Model: 225205KMI · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780511243
Version / Model
225205KMI
Catalog Number
225205KMI
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-05
Public Version
5
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
45f8df6d-c1f8-4d69-bdef-6b5a83c7e5b4
Distribution End Date
2026-12-31

Device Description

Katalyst Assembly Pliers

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
Yes
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 10381780511243

Customer Contacts