FDA UDI In Commercial Distribution 🇺🇸 United States

Professional Surgical Instruments Co., Inc.

DI: 00810058670533 · Model: 11-12000 · Professional Surgical Instruments Co., Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Professional Surgical Instruments Co., Inc.
Primary DI
00810058670533
Version / Model
11-12000
Company Name
Professional Surgical Instruments Co., Inc.
Labeler DUNS
197354343
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-12
Public Version
1
Public Version Date
2026-02-20
Public Version Status
New
Public Device Record Key
7cfb87b3-82c7-41b4-88d2-808c72a20ff6

Device Description

Double-Spring Plaster Nipper

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
No
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
LGG Instrument, Cast Application/Removal, Manual

GMDN Terms

Code Name
35140 Cast/plaster knife

Identifiers

Type ID
Primary 00810058670533

Device Sizes

Type Value Unit Text
Length 8 Inch