FDA UDI In Commercial Distribution 🇺🇸 United States

IS3618

DI: 10816336020486 · Model: IS3618 · NEOCHILD, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
IS3618
Primary DI
10816336020486
Version / Model
IS3618
Company Name
NEOCHILD, LLC
Labeler DUNS
022760922
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
f501bb80-d21c-4b27-ae6b-b74d061daf94

Device Description

Microbore Extension Set 36 inch. 0.18 priming vol.

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
Labeling does not contain MRI Safety Information
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
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 10816336021117
Primary 10816336020486

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K003854 000