FDA UDI In Commercial Distribution 🇺🇸 United States

INT, FirstWire

DI: 06950900959905 · Model: GW352AF · Shanghai Kindly Medical Instruments Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
1

Basic Information

Brand Name
INT, FirstWire
Primary DI
06950900959905
Version / Model
GW352AF
Company Name
Shanghai Kindly Medical Instruments Co., Ltd.
Labeler DUNS
420827639
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-18
Public Version
1
Public Version Date
2023-08-28
Public Version Status
New
Public Device Record Key
b248417c-fa6e-4740-b036-0641d89d8ea5

Device Description

0.035"*180cm, PTFE coating, angled tip

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQX Wire, Guide, Catheter

GMDN Terms

Code Name
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Package 16950900959902
Primary 06950900959905
Package 56950900959900
Package 26950900959909
Package 46950900959903

Premarket Submissions

Submission Number Supplement Number
K180177 000