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Butterfly Mobile Device Charging Kit

FDA UDI

Class II (US FDA UDI)

by Butterfly Network, Inc.

Identity

Trade Name
BUTTERFLY MOBILE DEVICE CHARGING KIT FDA UDI
Generic Name
Hand-held ultrasound imaging system, body-surface FDA UDI
Model / Reference
815-20072-00 FDA UDI

Identifiers

Primary DI / UDI-DI
00850027593111 FDA UDI
510(k) Number
K200980 FDA UDI
FDA Product Code
ITX FDA UDI
IYO FDA UDI
GMDN Term
Hand-held ultrasound imaging system, body-surface FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
892.1560 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand-held ultrasound imaging system, body-surface

Butterfly Mobile Device Charging Kit by Butterfly Network, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held ultrasound imaging system, body-surface.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Butterfly Network, Inc.

Sources (1)

  • FDA UDI e2f4beb2-e58a-4219-b78b-a9045a2a51e8 33 fields · synced Jun 9, 2026