FDA UDI In Commercial Distribution 🇺🇸 United States

Anodyne Surgical

DI: 00840516114842 · Model: 0022 · Psi/Eye-Ko, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Anodyne Surgical
Primary DI
00840516114842
Version / Model
0022
Company Name
Psi/Eye-Ko, Inc.
Labeler DUNS
063763833
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-28
Public Version
1
Public Version Date
2023-09-05
Public Version Status
New
Public Device Record Key
ab73dca1-00f7-4feb-b803-b8193fa4e3e9

Device Description

Sub Tenon Cannula 21g X 22mm (7/8") 7mm angled tip, tri port

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
["Ethylene Oxide", "Radiation Sterilization"]

Product Codes

Code Name
GAA Needle, Aspiration And Injection, Disposable

GMDN Terms

Code Name
47610 Ophthalmic needle, single-use

Identifiers

Type ID
Package 00840516118772
Primary 00840516114842
Package 00840516122649

Customer Contacts