← Back to catalogue

UltraStim X Blue

FDA UDIEUDAMED

Class II (US FDA UDI)

by Axelgaard Manufacturing Co., Ltd.

Identity

Trade Name
UltraStim X Blue FDA UDI
Generic Name
Transcutaneous electrical stimulation electrode, single-use FDA UDI
Model / Reference
USXPB5000 FDA UDI

Identifiers

Primary DI / UDI-DI
00851913006234 FDA UDI
510(k) Number
K130987 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Transcutaneous electrical stimulation 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

UltraStim X Blue by Axelgaard Manufacturing Co., Ltd. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 34546cc4-d20c-4a19-9649-c52290348607 36 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 2, 2026