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TENS Therapy Device

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref JPD-ES220Ref JPD-ES200

by Shenzhen Jumper Medical Equipment Co., Ltd

Identity

Trade Name
TENS Therapy Device EUDAMED
JUMPER FDA UDI
Generic Name
Craniofacial analgesia electrical stimulator FDA UDI
Device Name
TENS Therapy Device EUDAMED
Model / Reference
JPD-ES220 EUDAMED
JPD-ES200 EUDAMEDFDA UDI
JPD-ES210 FDA UDI

Identifiers

Primary DI / UDI-DI
06951740550352 EUDAMED
06951740550017 EUDAMEDFDA UDI
06951740550031 FDA UDI
Basic UDI-DI
69517405ES02R3 EUDAMED
Direct Marketing DI
06951740550352 EUDAMED
06951740550017 EUDAMED
FDA Product Code
NUH FDA UDI
EMDN Code
Z12062899 NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER EUDAMED
GMDN Term
Craniofacial analgesia electrical stimulator FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
882.5890 FDA UDI
Market of Registration
Ireland EUDAMED
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

TENS Therapy Device by Shenzhen Jumper Medical Equipment Co., Ltd — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
CN-MF-000014343
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (4)

  • EUDAMED a7e78faf-9316-46dd-ba7f-b51c9c54f836 61 fields · synced Oct 6, 2026
  • FDA UDI 7af9129b-b2ad-4ef4-ae20-4d23066c697b 32 fields · synced May 30, 2026
  • FDA UDI 05b05253-2183-4c86-9726-6ac2cb8c830d 32 fields · synced May 30, 2026
  • EUDAMED 682cf8cf-6e26-42b5-bfac-79b53872a66e 61 fields · synced Jul 16, 2026