FDA UDI In Commercial Distribution 🇺🇸 United States

SURGISTAR

DI: 00878799008220 · Model: 585151 · SURGISTAR, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SURGISTAR
Primary DI
00878799008220
Version / Model
585151
Company Name
SURGISTAR, INC.
Labeler DUNS
808865125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-02
Public Version
3
Public Version Date
2019-12-11
Public Version Status
Update
Public Device Record Key
bf0de18d-490a-4f1a-9401-0a7ecd6ffb63

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
Yes
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
OKS Lacrimal Stents And Intubation Sets

GMDN Terms

Code Name
47929 Lacrimal intubation set

Identifiers

Type ID
Package 10878799008227
Primary 00878799008220

Customer Contacts

Phone
17605982480