FDA UDI In Commercial Distribution 🇺🇸 United States

Single-use Biopsy Forceps

DI: 06971381252224 · Model: BFUW-2311 · SCIVITA 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
06971381252224
Version / Model
BFUW-2311
Company Name
SCIVITA MEDICAL TECHNOLOGY CO., LTD.
Labeler DUNS
544519831
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-24
Public Version
1
Public Version Date
2023-06-01
Public Version Status
New
Public Device Record Key
bcdb361f-5bf9-4a08-bba8-c48573802869

Device Description

The single-use biopsy forceps has no physical or electrical connection to the endoscopic system and enters the human body through the instrument channel of the endoscope.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
No
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 16971381252221
Primary 06971381252224
Package 26971381252228