FDA UDI In Commercial Distribution 🇺🇸 United States

Sensimatic™

DI: 00810000520756 · Model: D700SE230 · PARKELL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sensimatic™
Primary DI
00810000520756
Version / Model
D700SE230
Catalog Number
D700SE-230
Company Name
PARKELL, INC.
Labeler DUNS
009900424
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
99b87abc-24cd-4ab0-8eae-342ac82b2364

Device Description

D700SE Sensimatic™ Electrosurge 230volts

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKZ Unit, Electrosurgical, And Accessories, Dental

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00810000520756

Customer Contacts

Phone
6312491134