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DermaDam Synthetic Medium - 30pk

EUDAMEDFDA UDI

Class I (EU MDR)

Ref DENTALFUPIBLU01800530Model Dental Dam

by Four D Rubber Company Ltd

Identity

Trade Name
DermaDam Synthetic Medium - 30pk EUDAMED
Ultradent FDA UDI
Generic Name
Rubber dam, non-latex FDA UDI
Device Name
DermaDam Synthetic Medium - 30pk FDA UDI
Model / Reference
Dental Dam EUDAMED
DENTALFUPIBLU01800530 EUDAMED
Medium FDA UDI
Description
DermaDam Synthetic Medium - 30pk FDA UDI

Identifiers

Catalog Number
DENTALFUPIBLU01800530 FDA UDI
Primary DI / UDI-DI
05060748682017 EUDAMEDFDA UDI
Basic UDI-DI
5060748684DNLDD4J EUDAMED
FDA Product Code
EIE FDA UDI
EMDN Code
Y0504 ARMS, TORSO AND LEGS RE-EDUCATION DEVICES EUDAMED
GMDN Term
Rubber dam, non-latex FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.6300 FDA UDI
Market of Registration
Ireland 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rubber dam, Hevea-latex

DermaDam Synthetic Medium - 30pk by Four D Rubber Company Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rubber dam, Hevea-latex.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
GB-MF-000012178
Authorised Representative
DEVMED International Limited IE-AR-000011607

Sources (2)

  • EUDAMED 92e23396-f339-4b17-814e-3d4b8e6ca85c 61 fields · synced Jun 19, 2026
  • FDA UDI c6a5ab56-43bf-4cc5-ac0d-70eeb44a77ce 35 fields · synced May 29, 2026