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Renamel® Microhybrid Body B2

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 6061B2Model Dental Composites and Accessories - Dental composites => Hybrid filled Composites

by Deltamed GmbH

Identity

Trade Name
Renamel® Microhybrid Body B2 EUDAMED
Renamel® Microhybrid FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Renamel® Microhybrid Body B2, Syringe 5g FDA UDI
Model / Reference
Dental Composites and Accessories - Dental composites => Hybrid filled Composites EUDAMED
6061B2 EUDAMEDFDA UDI
Description
Renamel® Microhybrid Body B2, Syringe 5g FDA UDI

Identifiers

Catalog Number
6061B2 FDA UDI
Primary DI / UDI-DI
+EDEL6061B20 EUDAMED
EDEL6061B20 FDA UDI
Basic UDI-DI
++EDELTD03BUDI050024H9 EUDAMED
Direct Marketing DI
+EDEL6061B20 EUDAMED
510(k) Number
K222435 FDA UDI
FDA Product Code
EBF FDA UDI
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

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: Dental composite resin

Renamel® Microhybrid Body B2 by DeltaMed GmbH — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Deltamed GmbH
EUDAMED SRN
DE-MF-000007882

Sources (2)

  • EUDAMED bc16be66-406f-45e4-a629-9f2147100e6c 61 fields · synced Jun 18, 2026
  • FDA UDI 7a175592-ddf1-48c8-9bf4-3e7f84690641 36 fields · synced May 30, 2026