FDA UDI In Commercial Distribution 🇺🇸 United States

Endoch

DI: DBF1816A1362 · Model: DBF-1816AFSC · Endoch Inc
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Endoch
Primary DI
DBF1816A1362
Version / Model
DBF-1816AFSC
Catalog Number
DBF-1816AFSC
Company Name
Endoch Inc
Labeler DUNS
241382683
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-05
Public Version
1
Public Version Date
2019-06-13
Public Version Status
New
Public Device Record Key
08cc0111-35a0-495d-a0d7-c0cc3834317c

Device Description

DISPOSABLE BIOPSY FORCEPS, WITH SPIKE

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HFB Forceps, Biopsy, Gynecological
FCL Forceps, Biopsy, Non-Electric

GMDN Terms

Code Name
38711 Flexible endoscopic biopsy forceps, single-use

Identifiers

Type ID
Primary DBF1816A1362