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Aesculap

FDA UDI

Class II (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Cranial port/reservoir FDA UDI
Device Name
PED.SPRUNG RESERVOIR W/DISTAL CATHETER FDA UDI
Model / Reference
FV064T FDA UDI
Description
PED.SPRUNG RESERVOIR W/DISTAL CATHETER FDA UDI

Identifiers

Catalog Number
FV064T FDA UDI
Primary DI / UDI-DI
04041906142322 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Cranial port/reservoir FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5550 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cranial port/reservoir

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

Similar devices

Also classified as Cranial port/reservoir.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 0823e586-969f-4c5e-b330-0ff555f6ea7b 35 fields · synced Jun 8, 2026