FDA UDI In Commercial Distribution 🇺🇸 United States

HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL 5810 BLADE

DI: 00858736006144 · Model: 7023-5810 · HEMOSTATIX MEDICAL TECHNOLOGIES LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL 5810 BLADE
Primary DI
00858736006144
Version / Model
7023-5810
Catalog Number
7023-5810
Company Name
HEMOSTATIX MEDICAL TECHNOLOGIES LLC
Labeler DUNS
791221265
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-04-11
Public Version
1
Public Version Date
2019-04-19
Public Version Status
New
Public Device Record Key
06cdcd6b-95fc-4af9-b538-2edc49c810bd

Device Description

HEMOSTATIX THERMAL SCALPEL SYSTEM MODEL 5810 BLADE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
36136 Haemostatic knife

Identifiers

Type ID
Primary 00858736006144
Unit of Use 00858736006175

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K183009 000