FDA UDI In Commercial Distribution 🇺🇸 United States

NAMIC

DI: H749804270130 · Model: 80427013 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NAMIC
Primary DI
H749804270130
Version / Model
80427013
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
4
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
ab755e5f-3b26-41f9-982b-0eed2df53af4

Device Description

NAMIC Non-Vented 48" Trifurcated Fluid Delivery Set with Macro Drip Chamber

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
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FPA Set, administration, intravascular

GMDN Terms

Code Name
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package H749804270131
Primary H749804270130

Customer Contacts

Device Sizes

Type Value Unit Text
Length 48 Inch