FDA UDI In Commercial Distribution 🇺🇸 United States

Antrum Biopsy Forceps

DI: 00192896109384 · Model: 468-373 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Antrum Biopsy Forceps
Primary DI
00192896109384
Version / Model
468-373
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-12
Public Version
1
Public Version Date
2021-04-20
Public Version Status
New
Public Device Record Key
f23dc8e5-a74c-4297-99e3-dd337ca770e6

Device Description

Antrum Biopsy Forceps 4 X 6 Millimeters Vertical Cup Double Action Straight Jaw 140 Millimeters Working Length

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
KAE FORCEPS, ENT

GMDN Terms

Code Name
11775 Open-surgery biopsy forceps, reusable

Identifiers

Type ID
Primary 00192896109384

Customer Contacts