FDA UDI In Commercial Distribution 🇺🇸 United States

MICTEC ARCO KNOT PUSHER

DI: 00192896008014 · Model: 20918-92 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MICTEC ARCO KNOT PUSHER
Primary DI
00192896008014
Version / Model
20918-92
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-23
Public Version
1
Public Version Date
2018-09-24
Public Version Status
New
Public Device Record Key
15081552-f311-4476-9465-64cb205a95be

Device Description

MICTEC ARCO KNOT PUSHER

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", "Dry Heat Sterilization"]

Product Codes

Code Name
GCJ Laparoscope, General & Plastic Surgery

GMDN Terms

Code Name
45716 Suture knot pusher, reusable

Identifiers

Type ID
Previous B09920918920
Primary 00192896008014

Customer Contacts

Phone
8008217496

Premarket Submissions

Submission Number Supplement Number
K002877 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 4.5mm Diameter
Length 300 Millimeter