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Laguna Nigel 32'' 230v

FDA UDI

Class I (US FDA UDI)

by Silhouet-Tone Corporation

Identity

Trade Name
Laguna Nigel 32'' 230v FDA UDI
Generic Name
General examination/treatment chair, electric FDA UDI
Model / Reference
412031 FDA UDI

Identifiers

Catalog Number
412031 FDA UDI
Primary DI / UDI-DI
00667259000092 FDA UDI
FDA Product Code
LGX FDA UDI
GMDN Term
General examination/treatment chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Laguna Nigel 32'' 230v by Silhouet-Tone Corporation — Class I — 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 d79683f7-4171-4a77-8559-51d15198e49c 35 fields · synced Jun 8, 2026