FDA UDI In Commercial Distribution 🇺🇸 United States

Duckworth & Kent

DI: 05055313821632 · Model: DK7786 · DUCKWORTH AND KENT LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Duckworth & Kent
Primary DI
05055313821632
Version / Model
DK7786
Catalog Number
DK7786
Company Name
DUCKWORTH AND KENT LIMITED
Labeler DUNS
217182583
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-31
Public Version
3
Public Version Date
2023-08-21
Public Version Status
Update
Public Device Record Key
d0aa0ae2-3f06-423f-a160-d4c6ed704504

Device Description

Implantation System

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
KYB Lens, Guide, Intraocular

GMDN Terms

Code Name
47724 Manual intraocular lens injector, reusable

Identifiers

Type ID
Primary 05055313821632

Customer Contacts