FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327055467 · Model: 0504880500 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327055467
Version / Model
0504880500
Catalog Number
0504-880-500
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
5
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
7d7a3ddf-f809-4de0-8f03-5a24119a0ea5

Device Description

[Cutting Loop Electrode, Straight, 24 Fr ¿ 0 ¿, Only for use with Stryker Resectoscopes 0502-880-401, 0502-880-402, Do not use if package is damaged]

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FAJ Cystoscope and accessories, flexible/rigid

GMDN Terms

Code Name
61872 Endoscopic electrosurgical electrode, bipolar, single-use

Identifiers

Type ID
Package 37613327055468
Primary 07613327055467

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Degree: 0.0 Degree