FDA UDI In Commercial Distribution 🇺🇸 United States

SURGISTAR

DI: 00878799000736 · Model: 5501 · SURGISTAR, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SURGISTAR
Primary DI
00878799000736
Version / Model
5501
Company Name
SURGISTAR, INC.
Labeler DUNS
808865125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-08
Public Version
5
Public Version Date
2021-01-22
Public Version Status
Update
Public Device Record Key
d2eaf1e4-2012-45ea-a301-85b05d1c16b8

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GDX Scalpel, One-Piece

GMDN Terms

Code Name
37445 Manual scalpel blade, single-use

Identifiers

Type ID
Package 10878799000733
Primary 00878799000736

Customer Contacts

Phone
17605982480

Premarket Submissions

Submission Number Supplement Number
K923689 000