FDA UDI In Commercial Distribution 🇺🇸 United States

Anodyne Surgical

DI: 00840516129181 · Model: 8000(38) · Psi/Eye-Ko, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Anodyne Surgical
Primary DI
00840516129181
Version / Model
8000(38)
Company Name
Psi/Eye-Ko, Inc.
Labeler DUNS
063763833
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-24
Public Version
1
Public Version Date
2023-09-01
Public Version Status
New
Public Device Record Key
3da6f92b-d6bf-49ac-9ef9-2f556b5a3f86

Device Description

Lacrimal Cannula 25g X 38mm (1 1/2") Curved

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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
HMX Cannula, Ophthalmic

GMDN Terms

Code Name
10575 Lacrimal procedural cannula

Identifiers

Type ID
Package 00840516129686
Primary 00840516129181
Package 00840516130187

Customer Contacts