FDA UDI In Commercial Distribution 🇺🇸 United States

Omni-Tract®

DI: 10381780268437 · Model: 11182 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
Omni-Tract®
Primary DI
10381780268437
Version / Model
11182
Catalog Number
11182
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2018-10-23
Public Version
2
Public Version Date
2023-05-15
Public Version Status
Update
Public Device Record Key
72a5d87e-6da0-49e8-9dda-619ca8c6b334

Device Description

Omni-Tract® Heaney Retractor 10-1/2", Blade 1-1/8" X 3" Deep

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

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

GMDN Terms

Code Name
45181 Surgical retraction system, reusable

Identifiers

Type ID
Secondary M248111821
Primary 10381780268437
Unit of Use 00381780268430

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 13" Length