FDA UDI In Commercial Distribution 🇺🇸 United States

Angiotribe Forceps

DI: 00192896103405 · Model: 115-592 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Angiotribe Forceps
Primary DI
00192896103405
Version / Model
115-592
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-13
Public Version
1
Public Version Date
2020-07-21
Public Version Status
New
Public Device Record Key
a4f051a7-40a9-48cd-b03a-812e01a0b4d5

Device Description

Ferguson Angiotribe Forceps Straight 2 In 1 Groove

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
HTD FORCEPS

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Primary 00192896103405

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch