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Neobiotech Implant System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref SBS20

by Neobiotech. co., ltd

Identity

Trade Name
Bone Spreader EUDAMED
Neobiotech Implant System FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
Ø2.7 FDA UDI
Model / Reference
SBS20 EUDAMEDFDA UDI
Description
Ø2.7 FDA UDI

Identifiers

Primary DI / UDI-DI
08809276768353 EUDAMEDFDA UDI
Basic UDI-DI
B-08809276768353 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Poland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant system

Neobiotech Implant System by Neobiotech. co., ltd — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 18764c60-9be0-49d9-bc7c-ed2f710f626c 33 fields · synced Jun 19, 2026
  • EUDAMED b67764f7-c124-4b30-b4d5-40d8809a79cc 61 fields · synced Jun 19, 2026