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NeoShades® with Tabs Phototherapy Eye Shields - Micro

EUDAMEDFDA UDI

Class I (EU MDR)

Ref N720Model NeoShades®

by Neotech Products LLC

Identity

Trade Name
NeoShades® with Tabs Phototherapy Eye Shields - Micro EUDAMED
NeoShades® with Tabs FDA UDI
Generic Name
Eye mask FDA UDI
Device Name
NeoShades® EUDAMED
The NeoShades are indicated for use as eye protection during phototherapy sessions. They are intended for use on pediatric (neonates, infants and children) patients. FDA UDI
Model / Reference
NeoShades® EUDAMED
N720 EUDAMED
Micro FDA UDI
Description
The NeoShades are indicated for use as eye protection during phototherapy sessions. They are intended for use on pediatric (neonates, infants and children) patients. FDA UDI

Identifiers

Catalog Number
N720 FDA UDI
Primary DI / UDI-DI
10812594010221 EUDAMEDFDA UDI
Basic UDI-DI
081259401N72000M5 EUDAMED
FDA Product Code
FOK FDA UDI
EMDN Code
V0201 PHOTOTHERAPY MASKS EUDAMED
GMDN Term
Eye mask FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5270 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Phototherapy eye protector, reusable

NeoShades® with Tabs Phototherapy Eye Shields - Micro by Neotech Products LLC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Phototherapy eye protector, 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-000001895
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 1a654ffc-1b76-4741-87f9-2b4281754681 61 fields · synced Jun 19, 2026
  • FDA UDI b45c9c33-121a-4cf3-8db9-4126c4f97798 34 fields · synced May 29, 2026