FDA UDI In Commercial Distribution 🇺🇸 United States

INNOVA

DI: 00840682120272 · Model: IGS 540 ACT 001 · Hangwei GE Medical Systems Co., Ltd.
Product Codes
4
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INNOVA
Primary DI
00840682120272
Version / Model
IGS 540 ACT 001
Company Name
Hangwei GE Medical Systems Co., Ltd.
Labeler DUNS
654659689
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-10
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b24dfd8a-1ae4-4601-84b6-46d036099d78

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
No

Product Codes

Code Name
JAK System, x-ray, tomography, computed
JAA System, x-ray, fluoroscopic, image-intensified
OWB Interventional fluoroscopic x-ray system
IZI System, x-ray, angiographic

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital
37618 Full-body CT system

Identifiers

Type ID
Primary 00840682120272

Premarket Submissions

Submission Number Supplement Number
K091673 000