FDA UDI In Commercial Distribution 🇺🇸 United States

PRINCETON

DI: 00810158215719 · Model: R292-017340-003 · Princeton Medical Group, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRINCETON
Primary DI
00810158215719
Version / Model
R292-017340-003
Company Name
Princeton Medical Group, Inc.
Labeler DUNS
012857277
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-28
Public Version
1
Public Version Date
2025-08-05
Public Version Status
New
Public Device Record Key
ad567e5e-afa5-4255-8e7c-b819aaee5556

Device Description

BIOPSY FORCEPS AND GRASPER SEMI RIGID 5FR DOUBLE ACTION SPOON SERRATED 330MM STANDARD HANDLE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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

Product Codes

Code Name
GEN Forceps, General & Plastic Surgery

GMDN Terms

Code Name
38810 Flexible endoscopic biopsy forceps, reusable

Identifiers

Type ID
Primary 00810158215719