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Alcedo

FDA UDI

Class II (US FDA UDI)

by Suzhou Ennova Electronics Technology Co., Ltd

Identity

Trade Name
Alcedo FDA UDI
Generic Name
Neuromuscular transmission electrode FDA UDI
Model / Reference
P5050 FDA UDI

Identifiers

Primary DI / UDI-DI
06973265920076 FDA UDI
510(k) Number
K152648 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Neuromuscular transmission electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Neuromuscular transmission electrode

Alcedo by Suzhou Ennova Electronics Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neuromuscular transmission electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 95ffa300-3331-4662-9035-6db9ab86d106 33 fields · synced May 30, 2026