FDA UDI Not in Commercial Distribution 🇺🇸 United States

HEARTLINE ATRIAL BLADE SET

DI: 00192896070011 · Model: 2800-500-SET · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
HEARTLINE ATRIAL BLADE SET
Primary DI
00192896070011
Version / Model
2800-500-SET
Catalog Number
2800-500-SET
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-07
Public Version
5
Public Version Date
2023-07-19
Public Version Status
Update
Public Device Record Key
72ec1fc0-bbf5-4014-9323-af81e1e5eee5
Distribution End Date
2023-07-18

Device Description

HEARTLINE ATRIAL BLADE SET WITH HOLDER & INTRODUCER

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
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Previous B09928005000
Primary 00192896070011

Customer Contacts

Phone
800-821-7496