FDA UDI In Commercial Distribution 🇺🇸 United States

Bag Decanter

DI: 00813079020059 · Model: 9002 · REMINGTON MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Bag Decanter
Primary DI
00813079020059
Version / Model
9002
Catalog Number
9002
Company Name
REMINGTON MEDICAL, INC.
Labeler DUNS
788472314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d952cfd9-a6b4-4ac6-8f88-6e8e2e3d0181

Device Description

For aseptic decanting of I.V. fluids from flexible containers.

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
LHI Set, i.V. Fluid transfer

GMDN Terms

Code Name
60540 Intravenous fluid bag spike

Identifiers

Type ID
Package 10813079020056
Primary 00813079020059

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 35 degree