FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327059472 · Model: 0502555400 · STRYKER CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327059472
Version / Model
0502555400
Catalog Number
0502555400
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ef6cfcb8-6b0b-42d7-af06-3f2769412d76

Device Description

Biopsy Cup, Semi-flexible, 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
["Ethylene Oxide", "Moist Heat or Steam Sterilization"]

Product Codes

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

GMDN Terms

Code Name
38810 Flexible endoscopic biopsy forceps, reusable

Identifiers

Type ID
Primary 07613327059472

Customer Contacts

Device Sizes

Type Value Unit Text
Length 41.0 Centimeter