FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327060225 · Model: 0502880005 · STRYKER CORPORATION
Product Codes
4
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327060225
Version / Model
0502880005
Catalog Number
0502-880-005
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
2020-02-06
Public Version Status
Update
Public Device Record Key
f87e70e2-54d1-4217-ba2e-a5023d12795f

Device Description

Laser Bridge (for use with Straight Fire Laser)

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", "Hydrogen Peroxide", "Moist Heat or Steam Sterilization"]

Product Codes

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

GMDN Terms

Code Name
11265 Urethral dilator, reusable
17633 Urethrotome

Identifiers

Type ID
Primary 07613327060225

Customer Contacts