FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327059502 · Model: 0502555300 · STRYKER CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327059502
Version / Model
0502555300
Catalog Number
0502555300
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
2019-08-21
Public Version Status
Update
Public Device Record Key
5927ecf6-b699-4061-b55b-1d2f911c4e3d

Device Description

Semi-Flexible Scissors, 5 Fr.

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

Product Codes

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

GMDN Terms

Code Name
33199 Flexible endoscopic tissue manipulation forceps, single-use

Identifiers

Type ID
Primary 07613327059502

Customer Contacts

Device Sizes

Type Value Unit Text
Length 41.0 Centimeter