FDA UDI In Commercial Distribution 🇺🇸 United States

IPS e.max Press

DI: 07615208360851 · Model: 638152 · IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
5

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Basic Information

Brand Name
IPS e.max Press
Primary DI
07615208360851
Version / Model
638152
Catalog Number
638152
Company Name
IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Labeler DUNS
448015938
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2024-08-08
Public Version
1
Public Version Date
2024-08-16
Public Version Status
New
Public Device Record Key
ad566e96-6834-463c-a1b4-1b4678cec139

Device Description

IPS e.max Press Multi B2 5 pcs.

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EIH POWDER, PORCELAIN

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Package 07615208447682
Primary 07615208360851
Unit of Use 07615208512335
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