FDA UDI In Commercial Distribution 🇺🇸 United States

MaxGuard

DI: 10885403236242 · Model: ME2017 · BD Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MaxGuard
Primary DI
10885403236242
Version / Model
ME2017
Catalog Number
ME2017
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2025-07-04
Public Version Status
Update
Public Device Record Key
4eecb3be-cb78-4d13-878f-a28575b6f880

Device Description

Extension Set (ultra minibore) 152.4 cm (60 in)

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
FPA Set, administration, intravascular

GMDN Terms

Code Name
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Primary 10885403236242
Package 50885403236240

Customer Contacts

Device Sizes

Type Value Unit Text
Length 60 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 125 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Fragile, handle with care
Type
Special Storage Condition, Specify
Special Conditions
Storage Temperature
Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight