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Natus

FDA UDI

Class II (US FDA UDI)

by Technomed Engineering B.V.

Identity

Trade Name
Natus FDA UDI
Generic Name
Analytical scalp electrode, single-use FDA UDI
Device Name
Grass® Disposable Deep EEG Cup Electrode, Silver-Silver Chloride (AgAgCl) coated 10mm cup 1.5m wire 27pc FDA UDI
Model / Reference
038317 FDA UDI
Description
Grass® Disposable Deep EEG Cup Electrode, Silver-Silver Chloride (AgAgCl) coated 10mm cup 1.5m wire 27pc FDA UDI

Identifiers

Primary DI / UDI-DI
08720791371050 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Analytical scalp electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 10 Millimeter FDA UDI
Length — 1.5 Meter FDA UDI

Natus by Technomed Engineering B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ecc42531-5e31-4e19-93ef-1521c1b21585 36 fields · synced Jun 8, 2026