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Flexform Line

FDA UDI

Class I (US FDA UDI)

by H.s. Hospital Service Spa

Identity

Trade Name
FLEXFORM LINE FDA UDI
Generic Name
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
Device Name
HS GENERAL PURPOSE L 12FRX30CM FDA UDI
Model / Reference
HS GENERAL PURPOSE FDA UDI
Description
HS GENERAL PURPOSE L 12FRX30CM FDA UDI

Identifiers

Catalog Number
HSGPL1230 FDA UDI
Primary DI / UDI-DI
08033003349403 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Catheter Length — 30 Centimeter FDA UDI
Catheter Gauge — 12 French FDA UDI

Category: Multi-purpose percutaneous abdominothoracic drainage catheter

Flexform Line by H.s. Hospital Service Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose percutaneous abdominothoracic drainage catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
H.s. Hospital Service Spa

Sources (1)

  • FDA UDI 0960417b-2109-4bfe-ad65-785d68582b1f 36 fields · synced Jun 1, 2026