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Morpheus Pump Tube Set

FDA UDI

Class I (US FDA UDI)

by Promepla

Identity

Trade Name
MORPHEUS PUMP TUBE SET FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
7435 MORPHEUS PUMP TUBE SET FDA UDI
Model / Reference
ONG7435ST276 FDA UDI
Description
7435 MORPHEUS PUMP TUBE SET FDA UDI

Identifiers

Catalog Number
7435 FDA UDI
Primary DI / UDI-DI
03700512906186 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

Yes

FDA UDI

Category: Surgical irrigation/aspiration tubing set

Morpheus Pump Tube Set 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 bf8bdf39-6c98-4cff-a10e-40402ac4b81b 34 fields · synced May 30, 2026