FDA UDI In Commercial Distribution 🇺🇸 United States

NIO

DI: 07290008325080 · Model: NIO-P · WaisMed Ltd
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NIO
Primary DI
07290008325080
Version / Model
NIO-P
Company Name
WaisMed Ltd
Labeler DUNS
514619238
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-10
Public Version
1
Public Version Date
2020-08-18
Public Version Status
New
Public Device Record Key
a116d3f0-b097-4dfc-9afd-61eb46e3eb2b

Device Description

The NIO Pediatric device is indicated to provide intraosseous access in the proximal tibia as an alternative to IV access during emergencies. The device is for use in pediatric patients up to 12 years of age. New stabilizer for the pediatric device

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
18009 Intraosseous infusion kit

Identifiers

Type ID
Primary 07290008325080
Package 17290008325087

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160805 000