← Back to catalogue

Smart Drain Round Coaxial Drain Fr 28

FDA UDI

Class I (US FDA UDI)

by Redax Spa

Identity

Trade Name
Smart Drain Round Coaxial Drain Fr 28 FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Device Name
A sterile and single-use silicone device characterized by a drainage groove section and a round section portion. FDA UDI
Model / Reference
24730 FDA UDI
Description
A sterile and single-use silicone device characterized by a drainage groove section and a round section portion. FDA UDI

Identifiers

Catalog Number
24730 FDA UDI
Primary DI / UDI-DI
08034139297309 FDA UDI
FDA Product Code
GBP FDA UDI
GMDN Term
Closed-wound drain, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Closed-wound drain, non-bioabsorbable

Smart Drain Round Coaxial Drain Fr 28 by Redax Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drain, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Redax Spa

Sources (1)

  • FDA UDI ed6b9e16-c315-4784-8311-34a768549300 36 fields · synced May 30, 2026