FDA UDI In Commercial Distribution 🇺🇸 United States

Foerster Sponge Forceps

DI: 00192896105140 · Model: 123-608Q · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Foerster Sponge Forceps
Primary DI
00192896105140
Version / Model
123-608Q
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-28
Public Version
2
Public Version Date
2021-03-10
Public Version Status
Update
Public Device Record Key
f2f0f443-f062-4d30-945f-7cd708facc9c

Device Description

FOERSTER SPONGE FORCEPS CURVED SERRATED JAW QUANTUM

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
HTD FORCEPS

GMDN Terms

Code Name
11791 Dressing/utility forceps, scissors-like, reusable

Identifiers

Type ID
Primary 00192896105140

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8 Inch