FDA UDI In Commercial Distribution 🇺🇸 United States

PRINCETON

DI: 00810158217751 · Model: 49605-12 · Princeton Medical Group, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRINCETON
Primary DI
00810158217751
Version / Model
49605-12
Company Name
Princeton Medical Group, Inc.
Labeler DUNS
012857277
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-17
Public Version
1
Public Version Date
2025-10-27
Public Version Status
New
Public Device Record Key
ceda0535-ff4e-493c-89da-b5ef53abfad8

Device Description

RETRACTOR OBWEGESER FOR MOUTH JAW FACE CURVED DOWN 55X12MM 8.75"

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
GAD Retractor

GMDN Terms

Code Name
35314 Periocular/lacrimal retractor, hand-held, reusable

Identifiers

Type ID
Primary 00810158217751