FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327053807 · Model: 0502220530 · STRYKER CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327053807
Version / Model
0502220530
Catalog Number
0502-220-530
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
3078d8e9-ab9d-4ec8-a40a-c07a0bef8968

Device Description

Cutting Loop Electrode, .014 wire, 22 Fr ¿ 30 ¿

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

Product Codes

Code Name
KQT EVACUATOR, GASTRO-UROLOGY
FAS ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL
FAJ Cystoscope and accessories, flexible/rigid
HIH HYSTEROSCOPE (AND ACCESSORIES)

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 07613327053807

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Degree: 30.0 Degree