FDA UDI In Commercial Distribution 🇺🇸 United States

MediBag

DI: 00850000509238 · Model: 220582 · SUMMIT MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MediBag
Primary DI
00850000509238
Version / Model
220582
Catalog Number
220582
Company Name
SUMMIT MEDICAL PRODUCTS, INC.
Labeler DUNS
831704841
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-10
Public Version
1
Public Version Date
2021-06-18
Public Version Status
New
Public Device Record Key
7d60613e-71fd-4a9b-89c1-79305d61f192

Device Description

MediBag 420 ml w/ Nuraxial 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
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
KPE Container, I.V.

GMDN Terms

Code Name
35127 Intravenous administration bag/bottle

Identifiers

Type ID
Package 10850000509235
Primary 00850000509238
Package 20850000509232

Customer Contacts

Phone
8013521888

Premarket Submissions

Submission Number Supplement Number
K001287 000

Device Sizes

Type Value Unit Text
Total Volume 420 Milliliter