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Extraoral Headgear

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 155-106

by Great Lakes Dental Technologies

Identity

Trade Name
FACE CRIB PURPLE SMALL FDA UDI
Generic Name
Orthodontic extraoral headgear FDA UDI
Device Name
Extraoral Headgear EUDAMED
FACE CRIB PURPLE SMALL FDA UDI
Model / Reference
155-106 EUDAMEDFDA UDI
Description
FACE CRIB PURPLE SMALL FDA UDI

Identifiers

Catalog Number
155-106 FDA UDI
Primary DI / UDI-DI
+D7751551060 EUDAMED
D7751551060 FDA UDI
Basic UDI-DI
++D7751550288P EUDAMED
FDA Product Code
DZB FDA UDI
EMDN Code
Q010499 ORTHODONTIC DEVICES - OTHER EUDAMED
GMDN Term
Orthodontic extraoral headgear FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.5500 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

An Extraoral Headgear device is a medical device used for various purposes, including orthodontic treatment and pain management. This device is designed to provide comfortable and secure wear for patients.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000003408
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 30862aed-99c6-4e0c-907f-ec7daeda252a 61 fields · synced Aug 3, 2026
  • FDA UDI 8c5421a7-5c7e-47b3-9569-101b5e63c215 35 fields · synced May 30, 2026