FDA UDI In Commercial Distribution 🇺🇸 United States

TUBE SHAFT

DI: 00192896093430 · Model: 2901-109L · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TUBE SHAFT
Primary DI
00192896093430
Version / Model
2901-109L
Catalog Number
2901-109L
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
2
Public Version Date
2019-04-26
Public Version Status
Update
Public Device Record Key
67ed36fb-0e90-4c8e-bdff-41d24177e2d2

Device Description

TUBE SHAFT WITH LUER LOCK INSULATED

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
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
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
62061 Endoscopic electrosurgical electrode, monopolar, reusable

Identifiers

Type ID
Primary 00192896093430

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102921 000

Device Sizes

Type Value Unit Text
Length 450 Millimeter
Device Size Text, specify 10 Millimeter Diameter Shaft