FDA UDI Not in Commercial Distribution 🇺🇸 United States

Durette® IV, regular, refurb.

DI: 10697660002559 · Model: 21-555R · Oculo-Plastik Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Durette® IV, regular, refurb.
Primary DI
10697660002559
Version / Model
21-555R
Company Name
Oculo-Plastik Inc
Labeler DUNS
257382580
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-11
Public Version
2
Public Version Date
2022-03-25
Public Version Status
Update
Public Device Record Key
34437841-502d-4f74-93d1-0855e7bd496a
Distribution End Date
2022-03-24

Device Description

Stainless Steel Eye Cups for Durette® IV, regular (non glare) (refurbished) This stainless steel (surface treated) eye wear covers all wavelengths. USE ONLY WITH PURE LASERS OR PURE IPL SYSTEMS. DO NOT USE WITH SYSTEMS THAT ARE INTEGRATED WITH ELECTRIC CURRENT.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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

Product Codes

Code Name
IWS Shield, Eye, Radiological

GMDN Terms

Code Name
64273 Epiocular radiation shield, reusable

Identifiers

Type ID
Primary 10697660002559

Customer Contacts

Phone
514-381-3292