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ZYTO Hand Cradle

FDA UDI

Class II (US FDA UDI)

by ZYTO Technologies, Inc.

Identity

Trade Name
ZYTO Hand Cradle FDA UDI
Generic Name
Skin electrical conductance meter FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
B336000 FDA UDI
FDA Product Code
GZO FDA UDI
GMDN Term
Skin electrical conductance meter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1540 FDA UDI
Commercial Distribution
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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin electrical conductance meter

ZYTO Hand Cradle by ZYTO Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin electrical conductance meter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2cd9dcd5-1f04-4706-8cd2-1dcc8d523bc9 32 fields · synced May 31, 2026