FDA UDI In Commercial Distribution 🇺🇸 United States

EYE RETRACTOR

DI: 00192896012486 · Model: 10-5400 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EYE RETRACTOR
Primary DI
00192896012486
Version / Model
10-5400
Catalog Number
10-5400
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-03
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
0d71df5a-bc1a-447c-8b93-3d88c22d3ec0

Device Description

EYE RETRACTOR MALLEABLE STAINLESS STEEL

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
HNI Retractor, Ophthalmic

GMDN Terms

Code Name
32754 Ocular hook/spatula/manipulator, reusable

Identifiers

Type ID
Primary 00192896012486

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4.25 Inch