FDA UDI In Commercial Distribution 🇺🇸 United States

Laser kit

DI: 30697660002256 · Model: 21-330 · Oculo-Plastik Inc
Product Codes
3
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Laser kit
Primary DI
30697660002256
Version / Model
21-330
Company Name
Oculo-Plastik Inc
Labeler DUNS
257382580
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-07
Public Version
1
Public Version Date
2019-11-15
Public Version Status
New
Public Device Record Key
7c449f12-e7c2-4bef-887e-56f34ec68717

Device Description

Ocular Laser Shields (1 Regular Durette® II and 2 Medium Cox® II) (non glare) + spare headband & a case with 2 suction cups

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
No
Contains NRL
Yes
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

Product Codes

Code Name
KYE Inserter/Remover Contact Lens
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
IWS Shield, Eye, Radiological

GMDN Terms

Code Name
63962 Corneal shield applicator
64271 Radiation/mechanical corneal shield, reusable
64273 Epiocular radiation shield, reusable

Identifiers

Type ID
Primary 30697660002256

Customer Contacts

Phone
514-381-3292