FDA UDI Not in Commercial Distribution 🇺🇸 United States

GRI-BAG

DI: 08426314580816 · Model: 1000 AP · LABORATORIOS GRIFOLS SA
Product Codes
3
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
GRI-BAG
Primary DI
08426314580816
Version / Model
1000 AP
Company Name
LABORATORIOS GRIFOLS SA
Labeler DUNS
463720681
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-05
Public Version
5
Public Version Date
2021-10-26
Public Version Status
Update
Public Device Record Key
1e38e450-64c4-40d0-a80e-a75fb0a56064
Distribution End Date
2021-10-18

Device Description

GRI-BAG is a single-use, non-pyrogenic flexible empty container with incorporated 0.2 µ.m filter. It is supplied sterile in sealed peel-pack pouches and is available in volume capacities of 100 ml, 250 ml, 500 ml and 1000 ml. The GRI-BAG models have a twist-off valve output connector whereas the GRIBAG AP models have a conus vial output connector.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NEP System/Device, Pharmacy Compounding
FPB Filter, Infusion Line
KPE Container, I.V.

GMDN Terms

Code Name
35127 Intravenous administration bag/bottle
41646 Compounding transfer set

Identifiers

Type ID
Package 28426314580810
Primary 08426314580816

Premarket Submissions

Submission Number Supplement Number
K033916 000