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Prungo

FDA UDI

Class II (US FDA UDI)

by Hunan Ruijiu Technology Co., Ltd.

Identity

Trade Name
Prungo FDA UDI
Generic Name
Multi-modality physical therapy system, professional-use FDA UDI
Device Name
RL-100 FDA UDI
Model / Reference
RL-100 FDA UDI
Description
RL-100 FDA UDI

Identifiers

Primary DI / UDI-DI
06976510830038 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Multi-modality physical therapy system, professional-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Multi-modality physical therapy system, professional-use

Prungo by Hunan Ruijiu Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality physical therapy system, professional-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hunan Ruijiu Technology Co., Ltd.

Sources (1)

  • FDA UDI 16e163e4-12f9-4927-a015-248c7ffd9e5e 33 fields · synced Jun 8, 2026