FDA UDI In Commercial Distribution 🇺🇸 United States

SCHPENS FORKED ORBITAL RETRACTOR

DI: 00192896072299 · Model: 10-3880 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCHPENS FORKED ORBITAL RETRACTOR
Primary DI
00192896072299
Version / Model
10-3880
Catalog Number
10-3880
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-19
Public Version
2
Public Version Date
2023-06-22
Public Version Status
Update
Public Device Record Key
a1ce013a-4b8f-4d92-abf2-9cefee52bfce

Device Description

SCHPENS FORKED ORBITAL RETRACTOR

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
35349 Eyelid speculum, reusable

Identifiers

Type ID
Primary 00192896072299

Customer Contacts