FDA UDI In Commercial Distribution 🇺🇸 United States

PRINCETON

DI: 00810158211810 · Model: 11246-18 · Princeton Medical Group, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRINCETON
Primary DI
00810158211810
Version / Model
11246-18
Company Name
Princeton Medical Group, Inc.
Labeler DUNS
012857277
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-10
Public Version
1
Public Version Date
2024-04-18
Public Version Status
New
Public Device Record Key
32d1671d-e5a2-46be-8c48-989126d8553c

Device Description

FORCEPS FERRIS-SMITH 1X2 TEETH SERRATED 7"

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HTD Forceps

GMDN Terms

Code Name
36199 ENT soft-tissue cutting forceps

Identifiers

Type ID
Primary 00810158211810