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Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Surgical irrigation/aspiration pump, reusable FDA UDI
Device Name
JET IRRIGATION UNIT FDA UDI
Model / Reference
GN090 FDA UDI
Description
JET IRRIGATION UNIT FDA UDI

Identifiers

Catalog Number
GN090 FDA UDI
Primary DI / UDI-DI
04038653078103 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Surgical irrigation/aspiration pump, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation/aspiration pump, reusable

Aesculap by Aesculap, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration pump, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI f335c17c-3981-4aa7-b9f1-6d1ef4e27e5e 35 fields · synced May 31, 2026