FDA UDI In Commercial Distribution 🇺🇸 United States

SURGISTAR

DI: 00878799004635 · Model: 965562 · SURGISTAR, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

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Basic Information

Brand Name
SURGISTAR
Primary DI
00878799004635
Version / Model
965562
Catalog Number
LP7523
Company Name
SURGISTAR, INC.
Labeler DUNS
808865125
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-08
Public Version
4
Public Version Date
2020-02-06
Public Version Status
Update
Public Device Record Key
31abdff0-d726-4ae4-8ce2-c35c6366c4b2

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
EMF Knife, Surgical

GMDN Terms

Code Name
47569 Scalpel, single-use

Identifiers

Type ID
Package 10878799004632
Primary 00878799004635
Package 80878799004631
Package 90878799004638

Customer Contacts

Phone
17605982480