FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613154620241 · Model: 2296044021S1 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613154620241
Version / Model
2296044021S1
Catalog Number
2296-044-021S1
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-23
Public Version
7
Public Version Date
2022-01-17
Public Version Status
Update
Public Device Record Key
be71cc2a-2329-49ad-ad69-3914962b5122

Device Description

50.8mm x 18.9mm Straight Dermabrader, Non-Sterile

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GFE BRUSH, DERMABRASION, POWERED

GMDN Terms

Code Name
45553 Orthopaedic bur, single-use

Identifiers

Type ID
Primary 07613154620241

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 18.9 Millimeter
Length 50.8 Millimeter