FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613327147582 · Model: 0502142010 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327147582
Version / Model
0502142010
Catalog Number
502-142-010
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-14
Public Version
5
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
b7d66824-1781-4729-bd43-39a2ec829fb8
Distribution End Date
2020-02-05

Device Description

TMJ Endoscope, Autoclavable

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

Product Codes

Code Name
HRX Arthroscope

GMDN Terms

Code Name
34856 Rigid optical arthroscope, reusable

Identifiers

Type ID
Primary 07613327147582

Customer Contacts