FDA UDI In Commercial Distribution 🇺🇸 United States

Omni-Tract®

DI: 10381780272977 · Model: 3093P · INTEGRA LIFESCIENCES CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Omni-Tract®
Primary DI
10381780272977
Version / Model
3093P
Catalog Number
3093P
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-19
Public Version
3
Public Version Date
2023-05-25
Public Version Status
Update
Public Device Record Key
39361af5-d312-448d-9ef7-bb3d8df1996a

Device Description

Omni-Tract® Lechner-Harrington Live Blade, 5in X 3-1/2in (12.7cm x 8.9cm)

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
No

Product Codes

Code Name
FFO RETRACTOR, SELF-RETAINING
GAD RETRACTOR
FGN RETRACTOR, NON-SELF-RETAINING

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Secondary M2483093P1
Primary 10381780272977

Customer Contacts