FDA UDI In Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 20885403159975 · Model: MD1-1 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
500

Basic Information

Brand Name
V. Mueller
Primary DI
20885403159975
Version / Model
MD1-1
Catalog Number
MD1-1
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
Record Status
Published
Publish Date
2016-09-21
Public Version
6
Public Version Date
2022-03-07
Public Version Status
Update
Public Device Record Key
15c456b1-2135-4bb3-a47a-839fa86b9392

Device Description

V. Mueller GENESIS DATA CARDS 500/EA

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
63406 Device operating status label/tag, single-use

Identifiers

Type ID
Primary 20885403159975
Unit of Use 10885403159978

Customer Contacts