FDA UDI In Commercial Distribution 🇺🇸 United States

ATRIAL BLADE

DI: 00192896070059 · Model: 2800-506 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ATRIAL BLADE
Primary DI
00192896070059
Version / Model
2800-506
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-06
Public Version
3
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
14604f5c-57ef-49b6-bd6e-ee0b329d5bf2

Device Description

HEARTLINE ATRIAL BLADE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
FFO Retractor, Self-Retaining

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Previous B09928005060
Primary 00192896070059

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Device Size Text, specify 60mm x 35mm