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Sleeve

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 3DM00605NEOSS.10

by 3DIEMME srl

Identity

Trade Name
RealGUIDE Sleeve FDA UDI
Generic Name
Dental implantation drilling template guide-sleeve FDA UDI
Device Name
Sleeve EUDAMED
Model / Reference
3DM00605NEOSS.10 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
18050038830703 EUDAMEDFDA UDI
Basic UDI-DI
805003883SLVJJ EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010399 SURGICAL DENTAL DEVICES - OTHER EUDAMED
GMDN Term
Dental implantation drilling template guide-sleeve FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Sleeve by 3diemme Srl — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3DIEMME srl
EUDAMED SRN
IT-MF-000016005

Sources (2)

  • EUDAMED e3b588b4-f8de-4c97-8a42-3fc7f9aebe59 61 fields · synced Oct 6, 2026
  • FDA UDI 27890901-4a69-4d54-93ad-0a4cd1b28ae8 32 fields · synced May 29, 2026