FDA UDI In Commercial Distribution 🇺🇸 United States

Omni-Tract®

DI: 10381780271925 · Model: 11442 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Omni-Tract®
Primary DI
10381780271925
Version / Model
11442
Catalog Number
11442
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
750fac6a-5d3a-4de4-85bd-c6cdece3905b

Device Description

Omni-Tract® Kelly Swivel Retractor, Square Shaft, 2in x 3in (5.1cm x 7.6cm)

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

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Secondary M248114421
Primary 10381780271925

Customer Contacts