FDA UDI In Commercial Distribution 🇺🇸 United States

RETRACTOR ATRIAL RAKE

DI: 00192896070271 · Model: 2800-822 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RETRACTOR ATRIAL RAKE
Primary DI
00192896070271
Version / Model
2800-822
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
4
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
22564e0a-6d94-42ae-803d-1a5f6ef3643e

Device Description

HEARTLINE RETRACTOR ATRIAL RAKE

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 B09928008220
Primary 00192896070271

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Device Size Text, specify 29mm x 30mm