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DragonFly™ CHARGING SYSTEM

FDA UDI

Class II (US FDA UDI)

by Grace Medical, Inc.

Identity

Trade Name
DragonFly™ CHARGING SYSTEM FDA UDI
Generic Name
Noninvasive device battery charger FDA UDI
Device Name
DragonFly™ CHARGING SYSTEM INCLUDES US, UK, EU, AU ADAPTORS USED WITH 950-003 FOOTSWITCH FDA UDI
Model / Reference
950-005 FDA UDI
Description
DragonFly™ CHARGING SYSTEM INCLUDES US, UK, EU, AU ADAPTORS USED WITH 950-003 FOOTSWITCH FDA UDI

Identifiers

Primary DI / UDI-DI
00844505009874 FDA UDI
510(k) Number
K161376 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Noninvasive device battery charger FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 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

Yes

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

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: Noninvasive device battery charger

DragonFly™ CHARGING SYSTEM by Grace Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive device battery charger.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Grace Medical, Inc.

Sources (1)

  • FDA UDI 95d0da4d-2054-42b5-8378-8c05ae4c3b00 35 fields · synced May 30, 2026