FDA UDI In Commercial Distribution 🇺🇸 United States

Antrum Biopsy Forceps

DI: 00192896110632 · Model: 468-371 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Antrum Biopsy Forceps
Primary DI
00192896110632
Version / Model
468-371
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-21
Public Version
1
Public Version Date
2021-07-29
Public Version Status
New
Public Device Record Key
7e363493-4f06-4b05-8466-402f6b6e8897

Device Description

Antrum Biopsy Forceps 3.0 Millimeters X 5.0 Millimeters Oval Vertical Cup Double Action Straight Jaw

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
KAE FORCEPS, ENT

GMDN Terms

Code Name
11775 Open-surgery biopsy forceps, reusable

Identifiers

Type ID
Primary 00192896110632

Customer Contacts

Device Sizes

Type Value Unit Text
Length 140 Millimeter