FDA UDI In Commercial Distribution 🇺🇸 United States

KNUTSON URETHROGRAPHY CANNULA

DI: 00192896045453 · Model: 516-651 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KNUTSON URETHROGRAPHY CANNULA
Primary DI
00192896045453
Version / Model
516-651
Catalog Number
516-651
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
2
Public Version Date
2020-07-07
Public Version Status
Update
Public Device Record Key
9950bd49-1da8-437e-996d-c7862eb7dfdf

Device Description

KNUTSON URETHROGRAPHY CANNULA/RUBBER ACORN

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
Yes
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", "Dry Heat Sterilization"]

Product Codes

Code Name
GDJ CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
42797 Incontinence penis clamp, reusable

Identifiers

Type ID
Primary 00192896045453

Customer Contacts