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Nobel Biocare N1™

FDA UDI

Class II (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
Nobel Biocare N1™ FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
Healing Abutment Nobel Biocare N1™ Base Tri RP 3.8mm FDA UDI
Model / Reference
300989 FDA UDI
Description
Healing Abutment Nobel Biocare N1™ Base Tri RP 3.8mm FDA UDI

Identifiers

Catalog Number
300989 FDA UDI
Primary DI / UDI-DI
07332747162936 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Height — 3.800 Millimeter FDA UDI

Nobel Biocare N1™ by Nobel Biocare AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nobel Biocare AG

Sources (1)

  • FDA UDI 8be90df0-6362-4945-8bdf-c721d479d8e2 38 fields · synced May 31, 2026