FDA UDI In Commercial Distribution 🇺🇸 United States

HEARTLINE RETRACTOR BLADE

DI: 00192896093881 · Model: 2800-805 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HEARTLINE RETRACTOR BLADE
Primary DI
00192896093881
Version / Model
2800-805
Catalog Number
2800-805
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
1
Public Version Date
2019-03-15
Public Version Status
New
Public Device Record Key
57b08221-0bab-49f3-af20-22d0bd3d7830

Device Description

HEARTLINE RETRACTOR BLADE MORSE TYPE BLADES

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
FFO RETRACTOR, SELF-RETAINING

GMDN Terms

Code Name
46698 Intraocular retractor, single-use

Identifiers

Type ID
Primary 00192896093881

Customer Contacts

Device Sizes

Type Value Unit Text
Length 30 Millimeter