FDA UDI Not in Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403200359 · Model: MO10053 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
V. Mueller
Primary DI
10885403200359
Version / Model
MO10053
Catalog Number
MO10053
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-30
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
4b96c7f3-f040-4466-be29-f3f205482f6d
Distribution End Date
2021-10-12

Device Description

V. Mueller ORAL BONE FILE CROSS-SERRATED OVERALL LENGTH 7" (17.8CM)

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EMI FILE, BONE, SURGICAL

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 10885403200359

Customer Contacts