FDA UDI In Commercial Distribution 🇺🇸 United States

REMEX KA6

DI: 08800060100151 · Model: REMEX KA6 · REMEDI CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
REMEX KA6
Primary DI
08800060100151
Version / Model
REMEX KA6
Company Name
REMEDI CO.,LTD.
Labeler DUNS
690072489
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-13
Public Version
1
Public Version Date
2022-04-21
Public Version Status
New
Public Device Record Key
42d04806-193c-44a3-b1ed-9bcc1fb8985e

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IZI System, X-Ray, Angiographic

GMDN Terms

Code Name
37643 Portable basic diagnostic x-ray system, digital

Identifiers

Type ID
Primary 08800060100151

Premarket Submissions

Submission Number Supplement Number
K212144 000

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
76 – 106 KiloPascal
Type
Handling Environment Humidity
Temperature Range
5 – 85 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
15 – 40 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
76 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius