FDA UDI In Commercial Distribution 🇺🇸 United States

Needle 30G x 12,7 mm

DI: 08052276011992 · Model: 5200 · AKTIVE SRL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
Needle 30G x 12,7 mm
Primary DI
08052276011992
Version / Model
5200
Catalog Number
5200
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
89fa93a1-e4d7-4ac1-9a09-8ee51e49dfb6

Device Description

Needle 30G x 12,7 mm

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 08056477554845
Primary 08052276011992

Device Sizes

Type Value Unit Text
Device Size Text, specify GAUGE

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius