FDA UDI In Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403009341 · Model: AU11170 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
V. Mueller
Primary DI
10885403009341
Version / Model
AU11170
Catalog Number
AU11170
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-13
Public Version
3
Public Version Date
2024-02-02
Public Version Status
Update
Public Device Record Key
0e183cc4-7d4e-4fcd-b219-7a3992068ee6

Device Description

V. Mueller LEMPERT HEAVY ELEVATOR BLADE 5MM WIDE OVERALL LENGTH 7-3/8" (18.7CM)

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
No
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
KAD ELEVATOR, ENT

GMDN Terms

Code Name
35047 ENT elevator

Identifiers

Type ID
Primary 10885403009341

Customer Contacts