FDA UDI In Commercial Distribution 🇺🇸 United States

MaxGuard

DI: 10885403238420 · Model: MX9436 · BD Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
MaxGuard
Primary DI
10885403238420
Version / Model
MX9436
Catalog Number
MX9436
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-04
Public Version
7
Public Version Date
2024-08-14
Public Version Status
Update
Public Device Record Key
f5237a04-05cc-4a66-9f15-a1a657f78462

Device Description

15 DROP ADMIN SET W/3 NEEDLELES Y-SITES

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 10885403238420
Package 50885403238428

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature