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Whale

FDA UDI

Class II (US FDA UDI)

by Beijing East Whale Imaging Technology Co., Ltd.

Identity

Trade Name
WHALE FDA UDI
Generic Name
Mobile general-purpose fluoroscopic x-ray system, digital FDA UDI
Model / Reference
B6 FDA UDI

Identifiers

Primary DI / UDI-DI
06970528550063 FDA UDI
510(k) Number
K163429 FDA UDI
FDA Product Code
JAA FDA UDI
OXO FDA UDI
GMDN Term
Mobile general-purpose fluoroscopic x-ray system, digital FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 150 Kilogram FDA UDI
Height — 1760 Millimeter FDA UDI
Width — 670 Millimeter FDA UDI
Length — 1010 Millimeter FDA UDI
Weight — 529 Kilogram FDA UDI
Height — 2476 Millimeter FDA UDI
Width — 920 Millimeter FDA UDI
Length — 2820 Millimeter FDA UDI

Category: Mobile general-purpose fluoroscopic x-ray system, digital

Whale by Beijing East Whale Imaging Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile general-purpose fluoroscopic x-ray system, digital.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1dcbfd2e-1ff2-4376-80eb-7dc040c50ee0 35 fields · synced May 31, 2026