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Irrigation set for RTUP Diagnostic

FDA UDI

Class I (US FDA UDI)

by Promepla

Identity

Trade Name
Irrigation set for RTUP Diagnostic FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Model / Reference
GL0201T2S FDA UDI

Identifiers

Catalog Number
GL0201T2S FDA UDI
Primary DI / UDI-DI
03700512901518 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

Irrigation set for RTUP Diagnostic 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 14e3f5a0-ddc3-4955-8a4e-7ad147d75bdf 34 fields · synced Jun 7, 2026