FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327059885 · Model: 0502740052 · STRYKER CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327059885
Version / Model
0502740052
Catalog Number
0502-740-052
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
933b6e54-f29e-4a0e-a623-91a1f6b88cf1

Device Description

Hysteroscope Diagnostic Sheath (Outer)

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

Product Codes

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

GMDN Terms

Code Name
37086 Endoscope sheath, reusable

Identifiers

Type ID
Primary 07613327059885

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 4.0 Millimeter