FDA UDI In Commercial Distribution 🇺🇸 United States

BK PROBE

DI: 00310866002583 · Model: 26230 · PASCAL COMPANY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BK PROBE
Primary DI
00310866002583
Version / Model
26230
Company Name
PASCAL COMPANY, INC.
Labeler DUNS
009260217
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-20
Public Version
1
Public Version Date
2023-06-28
Public Version Status
New
Public Device Record Key
fdf6dd4f-ee3a-4388-b5da-dd6e3219df70

Device Description

PERIODONTAL PROBE/EXPLORER

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
EKB Explorer, Operative

GMDN Terms

Code Name
35812 Dental surgical probe, reusable

Identifiers

Type ID
Primary 00310866002583

Customer Contacts

Phone
8004268051