FDA UDI In Commercial Distribution 🇺🇸 United States

MT

DI: 06932503533355 · Model: IN12-254182302 · Micro-Tech (Nanjing) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MT
Primary DI
06932503533355
Version / Model
IN12-254182302
Company Name
Micro-Tech (Nanjing) Co., Ltd.
Labeler DUNS
530269083
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-28
Public Version
1
Public Version Date
2023-07-06
Public Version Status
New
Public Device Record Key
1c2c0091-1d3d-431e-a42e-7e82fa3d30a9

Device Description

POM inner tuber,Needle Length 4mm,with metal cap 25G*4*1.8*230,Shroat stucture

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
FBK Endoscopic Injection Needle, Gastroenterology-Urology

GMDN Terms

Code Name
45019 Submucosal injection needle

Identifiers

Type ID
Package 16932503533352
Primary 06932503533355
Package 26932503533359

Premarket Submissions

Submission Number Supplement Number
K150434 000