← Back to catalogue

Reliefband® Premier Slate Blue

FDA UDI

Class II (US FDA UDI)

by ReliefBand Technologies

Identity

Trade Name
Reliefband® Premier Slate Blue FDA UDI
Generic Name
Anti-nausea transcutaneous electrical nerve stimulation wristband FDA UDI
Device Name
Reliefband® Premier Slate Blue is a rechargeable, digital wearable device that is worn on the wrist. It consists of a hypoallergenic band with a control panel on top and two electrical contacts underneath. The two contacts must be placed firmly against the underside of your wrist at the P6 location. A fully charged battery will last for approximately 18 hours of continuous use at the mid-power level or below. FDA UDI
Model / Reference
2.0 Slate Blue FDA UDI
Description
Reliefband® Premier Slate Blue is a rechargeable, digital wearable device that is worn on the wrist. It consists of a hypoallergenic band with a control panel on top and two electrical contacts underneath. The two contacts must be placed firmly against the underside of your wrist at the P6 location. A fully charged battery will last for approximately 18 hours of continuous use at the mid-power level or below. FDA UDI

Identifiers

Catalog Number
2.0 FDA UDI
Primary DI / UDI-DI
00661168600039 FDA UDI
FDA Product Code
GZJ FDA UDI
GMDN Term
Anti-nausea transcutaneous electrical nerve stimulation wristband FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
Commercial Distribution
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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Category: Anti-nausea transcutaneous electrical nerve stimulation wristband

Reliefband® Premier Slate Blue by ReliefBand Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anti-nausea transcutaneous electrical nerve stimulation wristband.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
ReliefBand Technologies

Sources (1)

  • FDA UDI 8219621b-952b-4b73-99ab-904336d74c05 36 fields · synced Jun 8, 2026