FDA UDI In Commercial Distribution 🇺🇸 United States

Hydrodebrider®

DI: 00613994233295 · Model: 1913001 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hydrodebrider®
Primary DI
00613994233295
Version / Model
1913001
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7a1c9134-0417-4ece-8b9b-a2f135678bfe

Device Description

CONSOLE 1913001 HYDRODEBRIDER

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KMA IRRIGATOR, POWERED NASAL

GMDN Terms

Code Name
48010 Nasal lavage system

Identifiers

Type ID
Primary 00613994233295

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius