FDA UDI In Commercial Distribution 🇺🇸 United States

Sclerotherapy needle

DI: 06970401813902 · Model: MD-A-SY-2418-2108 · Zhejiang Chuangxiang Medical Technology Co., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sclerotherapy needle
Primary DI
06970401813902
Version / Model
MD-A-SY-2418-2108
Company Name
Zhejiang Chuangxiang Medical Technology Co., LTD.
Labeler DUNS
544434963
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-19
Public Version
1
Public Version Date
2022-08-29
Public Version Status
New
Public Device Record Key
324bece4-2a1f-439e-98f2-e0bb61f34515

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
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
FBK Endoscopic Injection Needle, Gastroenterology-Urology

GMDN Terms

Code Name
38825 General-purpose endoscopic needle, single-use

Identifiers

Type ID
Primary 06970401813902

Premarket Submissions

Submission Number Supplement Number
K212668 000