FDA UDI In Commercial Distribution 🇺🇸 United States

Well-Pex

DI: 08809254452304 · Model: WP102-K000 · VERICOM CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Well-Pex
Primary DI
08809254452304
Version / Model
WP102-K000
Company Name
VERICOM CO., LTD.
Labeler DUNS
689698269
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
c7e05c28-2137-4e30-bea4-7e632047d80f

Device Description

Calcium Hydroxide with Iodoform ; Well-Pex 2g x 1 syringe

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KIF Resin, Root Canal Filling

GMDN Terms

Code Name
36095 Endodontic filling/sealing material

Identifiers

Type ID
Primary 08809254452304

Customer Contacts

Phone
+82314412881

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 25 Degrees Celsius