FDA UDI In Commercial Distribution 🇺🇸 United States

SONTEC DOUBLE EDGE BLADE PACK

DI: 00192896099524 · Model: 11-5200 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SONTEC DOUBLE EDGE BLADE PACK
Primary DI
00192896099524
Version / Model
11-5200
Catalog Number
11-5200
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-18
Public Version
3
Public Version Date
2019-10-11
Public Version Status
Update
Public Device Record Key
a642364e-20c1-4b05-85a8-a27c220b7439

Device Description

SONTEC DOUBLE EDGE BLADE PACK CARBON STEEL

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
GFA Blade, Saw, General & Plastic Surgery, Surgical

GMDN Terms

Code Name
46724 Ophthalmic surgical instrument handle, manual

Identifiers

Type ID
Primary 00192896099524

Customer Contacts