FDA UDI In Commercial Distribution 🇺🇸 United States

ROCHESTER-OCHSNER FORCEPS

DI: 00192896021082 · Model: 115-526 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ROCHESTER-OCHSNER FORCEPS
Primary DI
00192896021082
Version / Model
115-526
Catalog Number
115-526
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-12
Public Version
3
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
3441f65b-12eb-4065-bf2e-46caf8621d0b

Device Description

ROCHESTER-OCHSNER FORCEPS CURVED SERRATED TIP

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
HTD FORCEPS

GMDN Terms

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

Identifiers

Type ID
Primary 00192896021082

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7.25 Inch
Device Size Text, specify 1 x 2 Teeth