FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327062946 · Model: 0502880219 · STRYKER CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327062946
Version / Model
0502880219
Catalog Number
0502-880-219
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
bb1501d8-5131-4746-8a87-afc69154b833

Device Description

19 Fr. Cystoscope Sheath

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

Product Codes

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

GMDN Terms

Code Name
37086 Endoscope sheath, reusable

Identifiers

Type ID
Primary 07613327062946

Customer Contacts