FDA UDI In Commercial Distribution 🇺🇸 United States

Foerster Sponge Forceps

DI: 00192896105539 · Model: 123-6181 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Foerster Sponge Forceps
Primary DI
00192896105539
Version / Model
123-6181
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-16
Public Version
1
Public Version Date
2020-11-24
Public Version Status
New
Public Device Record Key
6d918905-597d-44fe-98fb-dd27127a5f9a

Device Description

Foerster Sponge Forceps Straight Serrated 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
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
HTD FORCEPS

GMDN Terms

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

Identifiers

Type ID
Primary 00192896105539

Customer Contacts

Device Sizes

Type Value Unit Text
Length 12 Inch