FDA UDI In Commercial Distribution 🇺🇸 United States

MT

DI: 06932503533331 · Model: IN12-253232302 · Micro-Tech (Nanjing) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MT
Primary DI
06932503533331
Version / Model
IN12-253232302
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
2021-12-31
Public Version
1
Public Version Date
2022-01-10
Public Version Status
New
Public Device Record Key
1eb6fa3c-e325-42b6-9f8a-8d5cd46cdae6

Device Description

POM inner tuber,Needle Length 3mm,with metal cap 25G*3*2.3*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
Yes
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
Primary 06932503533331
Package 16932503533338
Package 26932503533335

Premarket Submissions

Submission Number Supplement Number
K150434 000