FDA UDI In Commercial Distribution 🇺🇸 United States

HydroBrader®

DI: 20681490051174 · Model: 1922100 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
HydroBrader®
Primary DI
20681490051174
Version / Model
1922100
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2017-09-09
Public Version
3
Public Version Date
2021-02-15
Public Version Status
Update
Public Device Record Key
d3c74863-2a3b-4cf0-a9d7-61e272bd1537

Device Description

DERMABRADER 1922100 HYDROBRADER 3PK CRSE

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GFF BUR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
34848 Metal/carbide ENT bur, single-use

Identifiers

Type ID
Primary 20681490051174
Unit of Use 00681490051170

Customer Contacts