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TURP Irrigation set for diagnostic – Use with Gravity

FDA UDI

Class I (US FDA UDI)

by Promepla

Identity

Trade Name
TURP Irrigation set for diagnostic – Use with Gravity FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Model / Reference
ONGR2000ST12 FDA UDI

Identifiers

Catalog Number
ONGR2000ST12 FDA UDI
Primary DI / UDI-DI
03700512900979 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

TURP Irrigation set for diagnostic – Use with Gravity 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

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Manufacturer

Manufacturer
Promepla

Sources (1)

  • FDA UDI 7382cb07-ea20-4988-9963-1588288966b2 34 fields · synced Jun 8, 2026