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Peak Universal Bond

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 4541

by Ultradent Products, Inc.

Identity

Trade Name
Peak Universal Bond & Peak SE Primer EUDAMED
Peak Universal Bond FDA UDI
Generic Name
Dentine adhesive FDA UDI
Device Name
Peak Universal Bond EUDAMED
Peak Universal Bond 4ml Bottle, Self-Etch Kit FDA UDI
Model / Reference
4541 EUDAMEDFDA UDI
Description
Peak Universal Bond 4ml Bottle, Self-Etch Kit FDA UDI

Identifiers

Catalog Number
4541 FDA UDI
Primary DI / UDI-DI
00883205045034 EUDAMED
00883205104274 FDA UDI
Basic UDI-DI
0883205-REF454172 EUDAMED
FDA Product Code
KLE FDA UDI
EMDN Code
Q01010104 DENTAL BONDING AGENTS EUDAMED
GMDN Term
Dentine adhesive FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
872.3200 FDA UDI
Medical Purpose
Intended for professional dental use to provide adhesive bonding between tooth structure and direct or indirect dental restorative materials during restorative and prosthetic dental procedures. EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Category: Dentine adhesive

Peak Universal Bond by Ultradent Products, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dentine adhesive.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 8f8cb499-9bbe-41d3-9913-1e2d82495036 36 fields · synced Jun 18, 2026
  • EUDAMED 19278835-1e16-4db2-a4ec-2084d2f532d3 61 fields · synced Jun 18, 2026