FDA UDI In Commercial Distribution 🇺🇸 United States

SeeStar

DI: 07350031353174 · Model: 13317 · Apriomed AB
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SeeStar
Primary DI
07350031353174
Version / Model
13317
Catalog Number
13317
Company Name
Apriomed AB
Labeler DUNS
631734758
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-04
Public Version
5
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
86b229d4-3db0-4035-a31e-792f5a2b1149
Distribution End Date
2026-02-26

Device Description

A passive guide for guided invasive access

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
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
GDF Guide, Needle, Surgical

GMDN Terms

Code Name
45018 Needle guide, single-use

Identifiers

Type ID
Package 17350031353171
Primary 07350031353174
Package 27350031353178

Customer Contacts

Phone
+46184301440

Device Sizes

Type Value Unit Text
Needle Gauge 17 Gauge