FDA UDI Not in Commercial Distribution 🇺🇸 United States

MaxGuard

DI: 10885403237713 · Model: MX9411 · BD Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MaxGuard
Primary DI
10885403237713
Version / Model
MX9411
Catalog Number
MX9411
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-04
Public Version
8
Public Version Date
2024-07-23
Public Version Status
Update
Public Device Record Key
77c48b3e-b292-47b7-9796-720c00423b3f
Distribution End Date
2023-02-01

Device Description

100-IN 20 DROP ADMIN SET NON-DEHP

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
No

Product Codes

Code Name
FPA Set, administration, intravascular

GMDN Terms

Code Name
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Primary 10885403237713
Package 50885403237711

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature