FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613327059205 · Model: 0502477131 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327059205
Version / Model
0502477131
Catalog Number
0502-477-131
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
e57b4a8d-78e2-480d-9a40-8b932af98a28
Distribution End Date
2016-10-15

Device Description

Arthroscope, Autoclavable, Reverse Cant

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
["Hydrogen Peroxide", "Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
34856 Rigid optical arthroscope, reusable

Identifiers

Type ID
Primary 07613327059205

Customer Contacts

Device Sizes

Type Value Unit Text
Angle 30.0 degree
Outer Diameter 4.0 Millimeter