FDA UDI In Commercial Distribution 🇺🇸 United States

BALFOUR LATERAL WIRE BLADE

DI: 00192896011489 · Model: 9-5203 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BALFOUR LATERAL WIRE BLADE
Primary DI
00192896011489
Version / Model
9-5203
Catalog Number
9-5203
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-02
Public Version
3
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
1f5f6c75-9369-4338-9228-2677618b9ba2

Device Description

DELUXE BALFOUR SIDE 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
FFO RETRACTOR, SELF-RETAINING

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896011489

Customer Contacts

Device Sizes

Type Value Unit Text
Length 3.5 Inch