FDA UDI In Commercial Distribution 🇺🇸 United States

Integra®

DI: 10381780248149 · Model: 12225300 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra®
Primary DI
10381780248149
Version / Model
12225300
Catalog Number
12225300
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-30
Public Version
4
Public Version Date
2023-02-20
Public Version Status
Update
Public Device Record Key
0b7f71af-5121-488a-baa9-689b0cf6ef87
Distribution End Date
2026-12-31

Device Description

Integra® External Fixation System The wire tensioner is used to apply tension to the wires after they are run through the bone and attached to the ring.

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
Yes
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
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Secondary M269122253001
Primary 10381780248149

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify .004 in opening