FDA UDI In Commercial Distribution 🇺🇸 United States

FEILCHENFELD SPLINTER FORCEPS

DI: 00192896023345 · Model: 138-025 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FEILCHENFELD SPLINTER FORCEPS
Primary DI
00192896023345
Version / Model
138-025
Catalog Number
138-025
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
f450cd73-09c9-40ed-8f75-975c12dff9e5

Device Description

FEILCHENFELD SPLINTER FORCEPS

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

Product Codes

Code Name
HTD FORCEPS

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 00192896023345

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4.5 Inch