FDA UDI In Commercial Distribution 🇺🇸 United States

DropSafe Sicura

DI: 00812383030877 · Model: 02099940220250 · PIKDARE SPA
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
DropSafe Sicura
Primary DI
00812383030877
Version / Model
02099940220250
Catalog Number
02099940220250
Company Name
PIKDARE SPA
Labeler DUNS
437816603
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-07-16
Public Version
1
Public Version Date
2023-07-24
Public Version Status
New
Public Device Record Key
4671e984-3e2b-4d48-9202-5b75114b7c40

Device Description

PASSIVE SAFETY NEEDLE DROPSAFE SICURA G22X25 5 P

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
No
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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 20812383030871
Primary 00812383030877
Unit of Use 10812383030928

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K223353 000

Device Sizes

Type Value Unit Text
Device Size Text, specify G22x25mm