FDA UDI In Commercial Distribution 🇺🇸 United States

Replacement attachments for Durette® III (set of 8)

DI: 20697660002402 · Model: 21-440 · Oculo-Plastik Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Replacement attachments for Durette® III (set of 8)
Primary DI
20697660002402
Version / Model
21-440
Company Name
Oculo-Plastik Inc
Labeler DUNS
257382580
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-11
Public Version
1
Public Version Date
2019-11-19
Public Version Status
New
Public Device Record Key
c352b701-6e95-40c4-af78-e01335840205

Device Description

Replacement attachments for Durette III (set of 8)

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
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
Liquid Chemical

Product Codes

Code Name
IWS Shield, Eye, Radiological

GMDN Terms

Code Name
64273 Epiocular radiation shield, reusable

Identifiers

Type ID
Primary 20697660002402

Customer Contacts

Phone
514-381-3292