FDA UDI In Commercial Distribution 🇺🇸 United States

Heartline Retractor Frame

DI: 00192896110083 · Model: 2800-800-SET · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Heartline Retractor Frame
Primary DI
00192896110083
Version / Model
2800-800-SET
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-28
Public Version
1
Public Version Date
2021-06-07
Public Version Status
New
Public Device Record Key
d132c12f-c450-49c5-b2ac-85016f039e2e

Device Description

Heartline Retractor Frame With Inserts 3 Sets Of Blades 18 Centimeter 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
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
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896110083

Customer Contacts