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TEE Articulated Arm

FDA UDI

Class II (US FDA UDI)

by Shenzhen Wisonic Medical Technology Co., Ltd.

Identity

Trade Name
TEE Articulated Arm FDA UDI
Generic Name
Frame/rail/pole device holder FDA UDI
Model / Reference
PHA-10 FDA UDI

Identifiers

Primary DI / UDI-DI
06971355420840 FDA UDI
510(k) Number
K210154 FDA UDI
FDA Product Code
IYN FDA UDI
GMDN Term
Frame/rail/pole device holder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1550 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Frame/rail/pole device holder

TEE Articulated Arm by Shenzhen Wisonic Medical Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Frame/rail/pole device holder.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a695b656-de46-47c6-966c-718969e05546 33 fields · synced Jun 6, 2026