FDA UDI In Commercial Distribution 🇺🇸 United States

BALFOUR CENTER BLADE

DI: 00192896097490 · Model: 220-605 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BALFOUR CENTER BLADE
Primary DI
00192896097490
Version / Model
220-605
Catalog Number
220-605
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-06
Public Version
1
Public Version Date
2019-06-14
Public Version Status
New
Public Device Record Key
3bc0fa44-4cb2-448e-a174-6ee74803b940

Device Description

BALFOUR CENTER BLADE WIDE SIZE

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
Yes
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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
GAD Retractor

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 00192896097490

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Depth 2.75 Inch
Width 3.25 Inch