FDA UDI In Commercial Distribution 🇺🇸 United States

MORRISON LENS LOOP & PROBE

DI: 00192896013537 · Model: 12-4480 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MORRISON LENS LOOP & PROBE
Primary DI
00192896013537
Version / Model
12-4480
Catalog Number
12-4480
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
3
Public Version Date
2019-10-07
Public Version Status
Update
Public Device Record Key
e9a4325e-d97f-4171-bb4c-4fb910a8583c

Device Description

MORRISON LENS LOOP & PROBE

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
HND Spatula, ophthalmic

GMDN Terms

Code Name
12319 Lens loop, reusable

Identifiers

Type ID
Primary 00192896013537

Customer Contacts

Device Sizes

Type Value Unit Text
Length 5.625 Inch
Device Size Text, specify 23 Gauge Probe