FDA UDI In Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403426285 · Model: ED1-3 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
V. Mueller
Primary DI
10885403426285
Version / Model
ED1-3
Catalog Number
ED1-3
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-17
Public Version
9
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
676e31a6-7a5c-4e23-a3f6-cb1ca1ed87de

Device Description

GENESIS COLOR END PLATE TOP, BROWN DUAL ACTION LATCH

Device Characteristics

Single Use
No
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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 10885403426285

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K844652 000