FDA UDI In Commercial Distribution 🇺🇸 United States

Suction Cups (12 units)

DI: 20697660002617 · Model: 23-012LF · Oculo-Plastik Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Suction Cups (12 units)
Primary DI
20697660002617
Version / Model
23-012LF
Company Name
Oculo-Plastik Inc
Labeler DUNS
257382580
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-08
Public Version
1
Public Version Date
2019-11-18
Public Version Status
New
Public Device Record Key
17e23afd-36a4-4cb7-893e-ccab83b7791d

Device Description

Latex-free Rubber Suction Cups (12 units)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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

Product Codes

Code Name
KYE Inserter/Remover Contact Lens

GMDN Terms

Code Name
63962 Corneal shield applicator

Identifiers

Type ID
Primary 20697660002617

Customer Contacts

Phone
514-381-3292