FDA UDI Not in Commercial Distribution 🇺🇸 United States

MaxGuard, MaxPlus

DI: 10885403236808 · Model: MP9004-NRC · BD Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MaxGuard, MaxPlus
Primary DI
10885403236808
Version / Model
MP9004-NRC
Catalog Number
MP9004-NRC
Company Name
BD Switzerland Sàrl
Labeler DUNS
482631558
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2024-07-23
Public Version Status
Update
Public Device Record Key
ed74a891-6057-4552-8dc9-23f3f4f73d8d
Distribution End Date
2023-02-01

Device Description

7 IN NON-DEHP MINIBORE SET

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
12170 Intravenous administration tubing extension set

Identifiers

Type ID
Package 20885403236805
Primary 10885403236808
Package 50885403236806

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Room Temperature