FDA UDI In Commercial Distribution 🇺🇸 United States

ARTHROSCOPIC GRASPING & BIOPSY RONGEUR FORCEPS

DI: 00192896056367 · Model: 1271-020 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ARTHROSCOPIC GRASPING & BIOPSY RONGEUR FORCEPS
Primary DI
00192896056367
Version / Model
1271-020
Catalog Number
1271-020
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
4
Public Version Date
2019-10-03
Public Version Status
Update
Public Device Record Key
0f5ed614-9dcc-4ffa-aacf-003a96bf1ac8

Device Description

ARTHROSCOPIC GRASPING & BIOPSY RONGEUR FORCEPS TUBULAR SHAFT SERRATED BITE

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
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
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
FCL FORCEPS, BIOPSY, NON-ELECTRIC

GMDN Terms

Code Name
11775 Open-surgery biopsy forceps, reusable

Identifiers

Type ID
Primary 00192896056367

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 4 Inch Shaft
Device Size Text, specify 2 Millimeter Tip