FDA UDI Not in Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403067372 · Model: 013.10 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
V. Mueller
Primary DI
10885403067372
Version / Model
013.10
Catalog Number
013.10
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2019-12-11
Public Version Status
Update
Public Device Record Key
a1675b69-c2cb-474e-b9b0-ca13d2275eb6
Distribution End Date
2019-01-23

Device Description

STORZ SNGL-STEM CUTTING LOOP 24FR 5/BX

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
FAS ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL

GMDN Terms

Code Name
35301 Resectoscope

Identifiers

Type ID
Package 20885403067379
Primary 10885403067372

Customer Contacts