FDA UDI In Commercial Distribution 🇺🇸 United States

OmniSight™

DI: 10381780167396 · Model: OTDB · INTEGRA LIFESCIENCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
OmniSight™
Primary DI
10381780167396
Version / Model
OTDB
Catalog Number
OTDB
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-08-25
Public Version
6
Public Version Date
2022-10-26
Public Version Status
Update
Public Device Record Key
81191099-2c3e-4d15-9ca2-cd877a8f5798

Device Description

Drapes, Sterile, OTS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MMP Cover, barrier, protective

GMDN Terms

Code Name
12535 Medical equipment drape, single-use

Identifiers

Type ID
Secondary M248OTDB1
Primary 10381780167396
Unit of Use 00381780167399

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010548 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not store above 150° F