FDA UDI In Commercial Distribution 🇺🇸 United States

HEALON DUET

DI: 05050474573574 · Model: 10290080 · JOHNSON & JOHNSON SURGICAL VISION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HEALON DUET
Primary DI
05050474573574
Version / Model
10290080
Catalog Number
10290080
Company Name
JOHNSON & JOHNSON SURGICAL VISION, INC.
Labeler DUNS
103021940
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-11-14
Public Version
4
Public Version Date
2020-02-26
Public Version Status
Update
Public Device Record Key
bb8003a9-83d5-4fb9-8263-304cda95f7cc

Device Description

HEALON DUET US

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LZP AID, SURGICAL, VISCOELASTIC

GMDN Terms

Code Name
35907 Vitreous/aqueous humour replacement medium, intraoperative

Identifiers

Type ID
Primary 05050474573574

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius