FDA UDI In Commercial Distribution 🇺🇸 United States

WELLS ENUCLEATION SPOON

DI: 00192896013612 · Model: 12-4750 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WELLS ENUCLEATION SPOON
Primary DI
00192896013612
Version / Model
12-4750
Catalog Number
12-4750
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
1
Public Version Date
2018-10-19
Public Version Status
New
Public Device Record Key
ad13604e-43e5-49c6-918b-2224eca121fa

Device Description

WELLS ENUCLEATION SPOON ANGLED HEAD

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
HNB Spoon, ophthalmic

GMDN Terms

Code Name
35153 Lens spoon

Identifiers

Type ID
Primary 00192896013612

Customer Contacts