FDA UDI In Commercial Distribution 🇺🇸 United States

Single Use Biopsy Forceps

DI: 06970401817238 · Model: MD-G-BF2403 · Zhejiang Chuangxiang Medical Technology Co., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Single Use Biopsy Forceps
Primary DI
06970401817238
Version / Model
MD-G-BF2403
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
2023-02-02
Public Version
1
Public Version Date
2023-02-10
Public Version Status
New
Public Device Record Key
ca36ebf9-8e1b-4d9f-9c21-43b02a165807

Device Description

without Plastic coated

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
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 16970401819567
Primary 06970401817238
Package 26970401818833