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Renonmed

FDA UDI

Class I (US FDA UDI)

by Zhejiang Renon Medical Instrument Co., Ltd.

Identity

Trade Name
RENONMED FDA UDI
Generic Name
Oral/upper respiratory tract specimen collection swab FDA UDI
Model / Reference
005 FDA UDI

Identifiers

Primary DI / UDI-DI
06975976450057 FDA UDI
FDA Product Code
KXG FDA UDI
GMDN Term
Oral/upper respiratory tract specimen collection swab FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oral/upper respiratory tract specimen collection swab

A comprehensive medical device directory resource for the RENONMED applicator, designed to collect oral/upper respiratory tract specimens for culture and analysis.

Similar devices

Also classified as Oral/upper respiratory tract specimen collection swab.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhejiang Renon Medical Instrument Co., Ltd.

Sources (1)

  • FDA UDI cc3b3727-1d4b-4eac-9b57-abee6f690a9b 32 fields · synced Aug 3, 2026