FDA UDI In Commercial Distribution 🇺🇸 United States

Skimmer®

DI: 00613994233257 · Model: 1882979HRE · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Skimmer®
Primary DI
00613994233257
Version / Model
1882979HRE
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-10
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
e3b3690c-1e26-4fa0-9731-b7c486ad97ee

Device Description

BLADE 1882979HRE SKIMMER M4 13CM 2.9MM

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
EQJ BUR, EAR, NOSE AND THROAT

GMDN Terms

Code Name
45527 Diamond ENT bur, single-use

Identifiers

Type ID
Primary 00613994233257

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 2.9 Millimeter
Length 13.0 Centimeter
Angle 15.0 degree