FDA UDI In Commercial Distribution 🇺🇸 United States

FeatherTouch®

DI: 00681490051088 · Model: 1922005 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FeatherTouch®
Primary DI
00681490051088
Version / Model
1922005
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-05
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
fc8aac16-2ea4-41d7-bf70-5bc172b5b992

Device Description

CONVERTER 1922005 FEATHERTOUCH AUTO RASP

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
No
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
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00681490051088

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K983025 000