FDA UDI In Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403113918 · Model: RH2090-002 · CAREFUSION 2200, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
V. Mueller
Primary DI
10885403113918
Version / Model
RH2090-002
Catalog Number
RH2090-002
Company Name
CAREFUSION 2200, INC
Labeler DUNS
832696038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
1baae5e3-3347-4c8b-9dd6-001cb2c2a826

Device Description

V. Mueller AUFRICHT NASAL RASP CURVED, CUTS DOWN BLADE 25 X 9MM WIDE OVERALL LENGTH 8" (20.3CM)

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
KBA RASP, NASAL

GMDN Terms

Code Name
35296 Nasal file/rasp

Identifiers

Type ID
Primary 10885403113918

Customer Contacts