FDA UDI In Commercial Distribution 🇺🇸 United States

BECKMAN RETRACTOR

DI: 00192896026759 · Model: 230-490 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BECKMAN RETRACTOR
Primary DI
00192896026759
Version / Model
230-490
Catalog Number
230-490
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-13
Public Version
2
Public Version Date
2022-11-01
Public Version Status
Update
Public Device Record Key
bb15a642-2d91-4ce9-9554-6e1efbca4922

Device Description

BECKMAN RETRACTOR HINGED SHARP TIPS

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
GAD Retractor

GMDN Terms

Code Name
45182 Self-retaining surgical retractor, reusable

Identifiers

Type ID
Primary 00192896026759

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10 Inch