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Senolo

FDA UDI

Class I (US FDA UDI)

by Jiangsu Senolo Medical Technology Co., Ltd.

Identity

Trade Name
Senolo FDA UDI
Generic Name
Cast construction material FDA UDI
Model / Reference
XE23 FDA UDI

Identifiers

Primary DI / UDI-DI
26952534451026 FDA UDI
FDA Product Code
ITG FDA UDI
GMDN Term
Cast construction material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cast construction material

Senolo by Jiangsu Senolo Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cast construction material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa0e3a6e-dbc3-4cf5-9860-d3b7dab3b432 32 fields · synced Jun 1, 2026