FDA UDI In Commercial Distribution 🇺🇸 United States

IONESQUE LEAFLET RETRACTOR

DI: 00192896067172 · Model: 2500-312 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IONESQUE LEAFLET RETRACTOR
Primary DI
00192896067172
Version / Model
2500-312
Catalog Number
2500-312
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-18
Public Version
2
Public Version Date
2020-02-06
Public Version Status
Update
Public Device Record Key
6f1a91b2-5132-4e94-a263-8e1b440998e8

Device Description

IONESQUE LEAFLET RETRACTOR DOUBLE ENDED ENDS

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
FGN RETRACTOR, NON-SELF-RETAINING

GMDN Terms

Code Name
13709 Rib spreader, reusable

Identifiers

Type ID
Primary 00192896067172

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10.5 Inch