FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 06932503561013 · Model: NGF03-11023180 · Micro-Tech (Nanjing) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
06932503561013
Version / Model
NGF03-11023180
Catalog Number
NGF03-11023180
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
2016-03-11
Public Version
4
Public Version Date
2021-05-17
Public Version Status
Update
Public Device Record Key
37901397-d2df-4cab-9bdd-62d10bd34327

Device Description

PE coated, Rat tooth, 2.3*1800mm

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
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered

GMDN Terms

Code Name
33199 Flexible endoscopic tissue manipulation forceps, single-use

Identifiers

Type ID
Package 26932503561017
Package 16932503561010
Primary 06932503561013
Package 36932503561014