FDA UDI In Commercial Distribution 🇺🇸 United States

SPENCER SUTURE SCISSORS

DI: 00192896047228 · Model: 1100-302 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPENCER SUTURE SCISSORS
Primary DI
00192896047228
Version / Model
1100-302
Catalog Number
1100-302
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
1
Public Version Date
2018-10-15
Public Version Status
New
Public Device Record Key
aa9d894e-c000-41a1-a44c-9a13403ce0bf

Device Description

SPENCER SUTURE SCISSORS STRAIGHT BLADE

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
Yes
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
LRW SCISSORS, GENERAL, SURGICAL

GMDN Terms

Code Name
13502 Suture scissors

Identifiers

Type ID
Primary 00192896047228

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6 Inch