FDA UDI Not in Commercial Distribution 🇺🇸 United States

BALFOUR RETRACTOR

DI: 00192896081819 · Model: 1100-614* · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BALFOUR RETRACTOR
Primary DI
00192896081819
Version / Model
1100-614*
Catalog Number
1100-614*
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-08
Public Version
3
Public Version Date
2023-08-10
Public Version Status
Update
Public Device Record Key
2fd2e0ed-908c-486d-9e7c-c3d1a2c05f8a
Distribution End Date
2023-08-09

Device Description

BALFOUR RETRACTOR LARGE SPREAD

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
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896081819

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 10.5 Inch