FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327063059 · Model: 0502880302 · STRYKER CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327063059
Version / Model
0502880302
Catalog Number
0502-880-302
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
4
Public Version Date
2019-03-11
Public Version Status
Update
Public Device Record Key
179835fb-aa2e-43a8-8d85-5371b9a17fdf

Device Description

Sweep Guide for Laser Cystoscope

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

GMDN Terms

Code Name
37086 Endoscope sheath, reusable

Identifiers

Type ID
Primary 07613327063059

Customer Contacts