FDA UDI In Commercial Distribution 🇺🇸 United States

NaviAid™ SPARK

DI: 07290018671528 · Model: SPARK · SMART MEDICAL SYSTEMS LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NaviAid™ SPARK
Primary DI
07290018671528
Version / Model
SPARK
Catalog Number
28-016
Company Name
SMART MEDICAL SYSTEMS LTD
Labeler DUNS
649905544
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-01
Public Version
1
Public Version Date
2020-12-09
Public Version Status
New
Public Device Record Key
6d0c5c42-e116-4793-9883-5788fed7b9b9

Device Description

An inflation system providing controlled inflation and deflation of the NaviAid™ AB balloon.

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
MR Unsafe
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
ODC Endoscope Channel Accessory

GMDN Terms

Code Name
46662 Catheter/overtube balloon inflator, reusable

Identifiers

Type ID
Primary 07290018671528

Customer Contacts

Phone
+97297444321

Premarket Submissions

Submission Number Supplement Number
K112106 000

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
.7 – 1.1 millibar
Type
Handling Environment Humidity
Temperature Range
30 – 85 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
.7 – 1.1 millibar
Type
Storage Environment Humidity
Temperature Range
0 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius