FDA UDI In Commercial Distribution 🇺🇸 United States

Nimbus

DI: 00817170020000 · Model: Nimbus · INFUTRONIX LLC
Product Codes
2
GMDN Terms
2
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Nimbus
Primary DI
00817170020000
Version / Model
Nimbus
Company Name
INFUTRONIX LLC
Labeler DUNS
079821136
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
86196cae-3c1d-447a-8c75-70e4b429aa87

Device Description

Ambulatory infusion pump

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MEA Pump, Infusion, Pca
FRN Pump, Infusion

GMDN Terms

Code Name
35932 Patient-controlled analgesia infusion pump
61514 Ambulatory non-insulin infusion pump, electronic

Identifiers

Type ID
Package 10817170020007
Primary 00817170020000
Package 20817170020004
Package 30817170020001