FDA UDI Not in Commercial Distribution 🇺🇸 United States

TUBE SHAFT INSULATED

DI: B0992901103L0 · Model: 2901-103L · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TUBE SHAFT INSULATED
Primary DI
B0992901103L0
Version / Model
2901-103L
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-19
Public Version
6
Public Version Date
2018-06-22
Public Version Status
Update
Public Device Record Key
6aa84e63-ead6-474f-899b-9f9fbe7d765a
Distribution End Date
2018-06-22

Device Description

TUBE SHAFT INSULATED 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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
32043 Laparoscopic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary B0992901103L0

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 450 Millimeter
Device Size Text, specify 5mm Shaft