FDA UDI In Commercial Distribution 🇺🇸 United States

Dual Bore Cannula 23G, 36mm

DI: 00805227602729 · Model: AK-0519/XL · AKTIVE SRL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Dual Bore Cannula 23G, 36mm
Primary DI
00805227602729
Version / Model
AK-0519/XL
Catalog Number
AK-0519/XL
Company Name
AKTIVE SRL
Labeler DUNS
433533053
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-12-19
Public Version
1
Public Version Date
2023-12-27
Public Version Status
New
Public Device Record Key
7fe3e512-6e5a-4f45-9a6f-9ab2c39807ad

Device Description

Dual Bore Cannula 23G, 36mm

Device Characteristics

Single Use
Yes
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
Yes
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
KYG Device, Irrigation, Ocular Surgery

GMDN Terms

Code Name
46705 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Identifiers

Type ID
Unit of Use 08056477559598
Primary 00805227602729

Device Sizes

Type Value Unit Text
Device Size Text, specify GAUGE

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius