FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613153155775 · Model: 07-10083 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613153155775
Version / Model
07-10083
Catalog Number
07-10083
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2022-02-17
Public Version Status
Update
Public Device Record Key
23f86c67-601d-4869-b71a-ec72ac55b102

Device Description

Gouge

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
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
35090 Surgical gouge

Identifiers

Type ID
Primary 07613153155775

Device Sizes

Type Value Unit Text
Length 15.0 Centimeter
Width 3.0 Millimeter