FDA UDI Not in Commercial Distribution 🇺🇸 United States

ProShape One Gutta Percha Primary

DI: 10810138822262 · Model: SDGP30061 · Endo Direct LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ProShape One Gutta Percha Primary
Primary DI
10810138822262
Version / Model
SDGP30061
Company Name
Endo Direct LLC
Labeler DUNS
125216703
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-15
Public Version
2
Public Version Date
2024-11-15
Public Version Status
Update
Public Device Record Key
7aed1afa-3908-4fd6-8d59-ac50b5e62156
Distribution End Date
2024-11-14

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKM Gutta-Percha

GMDN Terms

Code Name
45081 Synthetic gutta-percha

Identifiers

Type ID
Primary 10810138822262