FDA UDI In Commercial Distribution 🇺🇸 United States

SURGIPROS

DI: 00810143903980 · Model: 9027-58SP · Surgipros, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SURGIPROS
Primary DI
00810143903980
Version / Model
9027-58SP
Company Name
Surgipros, LLC
Labeler DUNS
058689193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-12
Public Version
1
Public Version Date
2023-12-20
Public Version Status
New
Public Device Record Key
c0caac22-55ac-4845-8de0-58ae0e7e4e97

Device Description

FEMORAL HREAD DRIVER

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
Yes
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

Product Codes

Code Name
HWA Impactor

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00810143903980

Customer Contacts

Phone
4109600452