FDA UDI Not in Commercial Distribution 🇺🇸 United States

PERITONEAL SCISSORS

DI: B09929013130 · Model: 2901-313 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERITONEAL SCISSORS
Primary DI
B09929013130
Version / Model
2901-313
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
9
Public Version Date
2022-09-23
Public Version Status
Update
Public Device Record Key
171a1c58-ffe2-4f66-8418-fc1c41793b91
Distribution End Date
2018-06-22

Device Description

PERITONEAL SCISSORS STRAIGHT SINGLE-ACTION JAW

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
38727 General-purpose surgical scissors, reusable

Identifiers

Type ID
Primary B09929013130

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K002877 000

Device Sizes

Type Value Unit Text
Length 210 Millimeter
Device Size Text, specify 3mm Shaft