FDA UDI In Commercial Distribution 🇺🇸 United States

Peri-Retrobulbar Needle Atkinson 23G x 32mm

DI: 08052276012036 · Model: 1641 · AKTIVE SRL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Peri-Retrobulbar Needle Atkinson 23G x 32mm
Primary DI
08052276012036
Version / Model
1641
Catalog Number
1641
Company Name
AKTIVE SRL
Labeler DUNS
433533053
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
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
709d221a-b844-43de-8caa-78b032672692

Device Description

Peri-Retrobulbar Needle Atkinson 23G x 32mm

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
HMX Cannula, Ophthalmic

GMDN Terms

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

Identifiers

Type ID
Unit of Use 08058340226620
Primary 08052276012036

Device Sizes

Type Value Unit Text
Device Size Text, specify GAUGE

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius