FDA UDI In Commercial Distribution 🇺🇸 United States

MT

DI: 46932503540108 · Model: NBF03-11023230-A · Micro-Tech (Nanjing) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
MT
Primary DI
46932503540108
Version / Model
NBF03-11023230-A
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
0e24b5fb-1f5b-4a6f-85a7-c97e82843ff0

Device Description

New handle, Oval, without spike, Tapered outer sheath, PE coated, Four-bar linkage, 2.3*2300 mm , 25 pcs in the box

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
Yes
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
FCL Forceps, Biopsy, Non-Electric

GMDN Terms

Code Name
38711 Flexible endoscopic biopsy forceps, single-use

Identifiers

Type ID
Package 56932503540105
Primary 46932503540108
Package 66932503540102
Package 76932503540109