FDA UDI In Commercial Distribution 🇺🇸 United States

ZERAMEX®

DI: 07640161390331 · Model: P36530 · CeramTec Schweiz GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ZERAMEX®
Primary DI
07640161390331
Version / Model
P36530
Catalog Number
P36530
Company Name
CeramTec Schweiz GmbH
Labeler DUNS
483229493
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-17
Public Version
5
Public Version Date
2024-12-11
Public Version Status
Update
Public Device Record Key
ba3f8b9b-5077-4278-bce1-6d2c11f35431

Device Description

ZERAMEX®P Provisorium RN (inkl. Screw)

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
NHA ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary 07640161390331

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152385 000
K163043 000

Device Sizes

Type Value Unit Text
Height 7 Millimeter
Outer Diameter 5.5 Millimeter
Device Size Text, specify Collar height
Height 1 Millimeter