FDA UDI In Commercial Distribution 🇺🇸 United States

Omni-Tract®

DI: 10381780270669 · Model: 4090 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Omni-Tract®
Primary DI
10381780270669
Version / Model
4090
Catalog Number
4090
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-23
Public Version
3
Public Version Date
2023-05-15
Public Version Status
Update
Public Device Record Key
1b9fe854-d2bb-4965-916e-d99c406aeeac

Device Description

Omni-Tract® Omni-Ring, 12in x 18in (30.5cm x 45.7cm) Oval

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

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Secondary M24840901
Primary 10381780270669

Customer Contacts