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100x10 8mm allergEAZE Patch Test Chambers

by SmartPractice United States EUDAMED510(k)GUDID

Ref AL67830GENModel allergEAZE Patch Test Chambers Product code KXFEMDN A99

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0854498007AL71200Z9 Basic UDI-DIDate28 Apr 2022RegisteredStatusActive
United StatesGUDID listing GUDID Number00854498007108 UDI-DIDate2 Dec 2020ListedStatusIn distribution
United StatesFDA 510(k) 510(k) NumberK063160 Date22 Dec 2006IssuedStatusActive

Coverage

2 jurisdictions

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaSwedenFinlandFinlandUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaSwedenFinlandFinlandUnited States of AmericaUnited States of AmericaUnited States of AmericaSwedenSwedenLatviaEstoniaUnited States of AmericaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaFranceFranceAustriaHungaryRomaniaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaFranceFranceSloveniaBulgariaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaPortugalSpainSpainItalyUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaSpainSpainCroatiaGreeceUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaMaltaCyprusUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered
  • United States FDA 510(k) Active
  • European Union CE/MDR Active

Recalls: none on record (FDA, checked 24 Oct 2026)

Certificates: none listed in EUDAMED

Specification

EUDAMED · 510(k) · GUDID · synced 24 Oct 2026

Trade Name
100x10 8mm allergEAZE Patch Test Chambers EUDAMED
SmartPractice GUDID
Generic Name
Allergy testing adhesive strip, epicutaneous
Model / Ref / Catalog
allergEAZE Patch Test Chambers EUDAMED
AL67830GEN EUDAMED
AL71200 GUDID
Primary DI / UDI-DI
00854498007108
Basic UDI-DI
0854498007AL71200Z9
Unit of Use DI
10854498007105
510(k) Number
FDA Product Code
KXF
EMDN Code
A99 Devices for administration, withdrawal and collection - other
GMDN Term
Allergy testing adhesive strip, epicutaneous
Device Class
Class I
Regulation Number
880.6025
Market of Registration
Germany
Commercial Distribution
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
allergEAZE Patch Test Chambers
AL67830GEN
GUDID
AL71200

Manufacturer details

EUDAMED SRN
US-MF-000005657
Authorised representative
Dr. Ebeling & Assoc. GmbH DE-AR-000000003

Other devices from SmartPractice

See all devices from SmartPractice →

Properties & raw data

Show properties, registry sources and raw records
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
Other properties (20)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No

Sources (3)

  • EUDAMED b603205f-44d8-4e29-a0cc-5c190fb3d92a 61 fields · synced 24 Oct 2026
  • FDA UDI 160258a2-f905-43b9-8c2d-e126fd706e2c 36 fields · synced 30 May 2026
  • FDA 510(k) K063160 1 fields · synced 18 May 2026