FDA UDI In Commercial Distribution 🇺🇸 United States

REFORM

DI: 00380652257039 · Model: 8065225703 · Alcon Laboratories, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REFORM
Primary DI
00380652257039
Version / Model
8065225703
Catalog Number
ACTR10
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
3
Public Version Date
2018-05-17
Public Version Status
Update
Public Device Record Key
f00adc6e-f073-475a-8019-f7a982a0f33e

Device Description

REFORM CAPSULAR TENSION RING 12.3/10MM The ALCON ReFORM Capsular Tension Ring is a sterile, non-optical ocular implant, manufactured from a single piece of PMMA(POlymethylmethacrylate).

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
MRJ Ring, Endocapsular

GMDN Terms

Code Name
42839 Capsular tension ring

Identifiers

Type ID
Primary 00380652257039

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Outer diameter compressed : 10.0 Millimeter
Outer Diameter 12.3 Millimeter