FDA UDI In Commercial Distribution 🇺🇸 United States

OMNI

DI: 00812231032862 · Model: 83-10-4120 · SANTA BARBARA IMAGING SYSTEMS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
OMNI
Primary DI
00812231032862
Version / Model
83-10-4120
Catalog Number
83-10-4120
Company Name
SANTA BARBARA IMAGING SYSTEMS, INC.
Labeler DUNS
065016344
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-26
Public Version
1
Public Version Date
2020-09-03
Public Version Status
New
Public Device Record Key
f2592fd0-1c48-4086-ad6d-e55e54ee7e9b

Device Description

4K UHD CAMERA HEAD, INTEGRATED, 1CMOS, HOLOGIC

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
GCJ Laparoscope, General & Plastic Surgery

GMDN Terms

Code Name
35958 Endoscope video camera

Identifiers

Type ID
Package 00812231032978
Primary 00812231032862

Customer Contacts

Phone
805-770-2110