FDA UDI In Commercial Distribution 🇺🇸 United States

BENNETT RETRACTOR

DI: 00192896097575 · Model: 1103-862A · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BENNETT RETRACTOR
Primary DI
00192896097575
Version / Model
1103-862A
Catalog Number
1103-862A
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-12
Public Version
3
Public Version Date
2023-07-21
Public Version Status
Update
Public Device Record Key
653a3bc1-c9dc-4e2f-a9cb-30dccfc6299a

Device Description

BENNETT RETRACTOR CROSS ACTION BLUNT SELF RETAINING TIP

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
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896097575

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Device Size Text, specify 3 Inch Spread
Length 4 Inch