FDA UDI In Commercial Distribution 🇺🇸 United States

V. Mueller

DI: 10885403113673 · Model: RH2000-4 · STERIS CORPORATION
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
10885403113673
Version / Model
RH2000-4
Catalog Number
RH20004
Company Name
STERIS CORPORATION
Labeler DUNS
021599373
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
5
Public Version Date
2024-08-28
Public Version Status
Update
Public Device Record Key
3a8a054f-4e4f-4931-a831-29ea5c45f0be

Device Description

V. Mueller DIAMOND RASP CURVED MEDIUM GRIT OVERALL LENGTH 7-1/4 inches 18.4CM

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
13291 Plastic surgery file/rasp

Identifiers

Type ID
Primary 10885403113673

Customer Contacts