← Back to catalogue

Urology TURP Gravity Tubing

FDA UDI

Class I (US FDA UDI)

by Promepla

Identity

Trade Name
Urology TURP Gravity Tubing FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Irrigation set for TURP / diagnostic FDA UDI
Model / Reference
GB1TURP FDA UDI
Description
Irrigation set for TURP / diagnostic FDA UDI

Identifiers

Catalog Number
ONGR2000ST12 FDA UDI
Primary DI / UDI-DI
03700512902003 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set 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: Surgical irrigation/aspiration tubing set

Urology TURP Gravity Tubing by Promepla — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

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
Promepla

Sources (1)

  • FDA UDI cd484b3a-b659-4523-8649-a1e10215837b 34 fields · synced Jun 1, 2026