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Barnhart 5-6 Xp (3/8) Ss

EUDAMEDFDA UDI

Class I (EU MDR)

Ref AECB5-6XPZ

by American Eagle Instruments

Identity

Trade Name
BARNHART 5-6 XP (3/8) SS EUDAMED
American Eagle Instruments FDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
Periodontal Curette EUDAMED
BARNHART 5-6 XP (3/8) SS FDA UDI
Model / Reference
AECB5-6XPZ EUDAMEDFDA UDI
Description
BARNHART 5-6 XP (3/8) SS FDA UDI

Identifiers

Catalog Number
AECB5-6XPZ FDA UDI
Primary DI / UDI-DI
00841013103278 EUDAMEDFDA UDI
Basic UDI-DI
0841013141660EMSA737883F3 EUDAMED
FDA Product Code
EMS FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Periodontal curette FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 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

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

FDA UDI

Category: Surgical retraction system, reusable

Barnhart 5-6 Xp (3/8) Ss by American Eagle Instruments — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000018222
Authorised Representative
Young Microbrush Ireland Ltd IE-AR-000011249

Sources (2)

  • EUDAMED 4b59576b-fecb-4e20-bcad-05d5ce92e73f 61 fields · synced Jun 17, 2026
  • FDA UDI f5fb8d3a-29ce-48c6-9e47-7716d01d7dca 34 fields · synced May 30, 2026