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Grass

FDA UDI

Class II (US FDA UDI)

by Natus Manufacturing Limited

Identity

Trade Name
Grass FDA UDI
Generic Name
Nasopharyngeal electrode FDA UDI
Device Name
Genuine GRASS Nasopharyngeal Electrodes15cm- Reusable FDA UDI
Model / Reference
F-EPG-G-15CM-48 FDA UDI
Description
Genuine GRASS Nasopharyngeal Electrodes15cm- Reusable FDA UDI

Identifiers

Primary DI / UDI-DI
00382830017282 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Nasopharyngeal electrode 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Grass by Natus Manufacturing Limited — 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 817d8d47-0391-4858-ac5b-a46a7e375761 34 fields · synced May 30, 2026