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Dyonics

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
DYONICS FDA UDI
Generic Name
Secondary battery FDA UDI
Device Name
DYONICS LRG NIMH BATTERY (AUTOCLAVABLE) FDA UDI
Model / Reference
72204113 FDA UDI
Description
DYONICS LRG NIMH BATTERY (AUTOCLAVABLE) FDA UDI

Identifiers

Catalog Number
72204113 FDA UDI
Primary DI / UDI-DI
00885554033441 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Secondary battery FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Secondary battery

Dyonics by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secondary battery.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 42f8c5cd-6b64-486d-a0ac-c35daef67edc 35 fields · synced Jun 8, 2026