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SET ZZ BASE MS-S-ICOTH Wide (Impression coping open tray hex and Screw

FDA UDI

Class I (US FDA UDI)

by Zirkonzahn GmbH

Identity

Trade Name
SET ZZ BASE MS-S-ICOTH Wide (Impression coping open tray hex and Screw FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, reusable FDA UDI
Device Name
Compatible with MIS SEVEN implants Set consisting of: 1x Impression coping HEX 1x Screw for Impression coping 1x Driver for Impression coping open tray FDA UDI
Model / Reference
BSAQ1642 FDA UDI
Description
Compatible with MIS SEVEN implants Set consisting of: 1x Impression coping HEX 1x Screw for Impression coping 1x Driver for Impression coping open tray FDA UDI

Identifiers

Primary DI / UDI-DI
D800BSAQ1642 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, temporary, preformed, reusable

SET ZZ BASE MS-S-ICOTH Wide (Impression coping open tray hex and Screw by Zirkonzahn GmbH — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zirkonzahn GmbH

Sources (1)

  • FDA UDI 4ec35cb2-7718-4fb3-bca1-dece2b18cf12 34 fields · synced May 30, 2026