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Neobiotech Implant System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref ACMSI60S

by Neobiotech. co., ltd

Identity

Trade Name
AutoChip Maker Stopper EUDAMED
Neobiotech Implant System FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
Ø6.0, L:17.7mm, Short FDA UDI
Model / Reference
ACMSI60S EUDAMEDFDA UDI
Description
Ø6.0, L:17.7mm, Short FDA UDI

Identifiers

Primary DI / UDI-DI
08809276762894 EUDAMEDFDA UDI
Basic UDI-DI
B-08809276762894 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

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

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 3d2ad8a8-4e5c-4f86-b528-a2782539b22f 33 fields · synced Jun 19, 2026
  • EUDAMED 135360ad-220c-4124-99e5-5c64f186ec09 61 fields · synced Jun 19, 2026