FDA UDI In Commercial Distribution 🇺🇸 United States

TUBE SHAFT INSULATED INSERT

DI: 00192896007437 · Model: 2901-105L · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TUBE SHAFT INSULATED INSERT
Primary DI
00192896007437
Version / Model
2901-105L
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-22
Public Version
3
Public Version Date
2019-05-08
Public Version Status
Update
Public Device Record Key
41e4ea72-f789-4309-a586-e93871e344aa

Device Description

TUBE SHAFT INSULATED INSERT WITH LUER LOCK

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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
62061 Endoscopic electrosurgical electrode, monopolar, reusable

Identifiers

Type ID
Previous B0992901105L0
Primary 00192896007437

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K102921 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 10mm Shaft
Device Size Text, specify Insulation reduction to 5mm Shaft
Length 330 Millimeter