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i-Sil Heavy Body

EUDAMEDFDA UDI

Class I (EU MDR)

Ref #7307P04

by Spident

Identity

Trade Name
i-Sil Heavy Body EUDAMED
I-SIL Heavy Body Regular Set FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
i-Sil Heavy Body EUDAMED
Vinyl Polysiloxane Impression Material FDA UDI
Model / Reference
#7307P04 EUDAMED
102-0401 FDA UDI
Description
Vinyl Polysiloxane Impression Material FDA UDI

Identifiers

Primary DI / UDI-DI
08809262955033 EUDAMEDFDA UDI
Basic UDI-DI
880926295HBZQ EUDAMED
Direct Marketing DI
08809262955033 EUDAMED
FDA Product Code
ELW FDA UDI
EMDN Code
Q01020102 DENTAL IMPRESSION VINYLSILOXANS EUDAMED
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Silicone dental impression material

i-Sil Heavy Body by Spident — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spident
EUDAMED SRN
KR-MF-000008691
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (2)

  • EUDAMED 0173e6dc-2abb-4f9e-9d48-cbbdf1143135 61 fields · synced Jun 8, 2026
  • FDA UDI ca01be33-9706-41bf-9c34-41beb4eb17d0 34 fields · synced May 29, 2026