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Total Abscession

FDA UDI

Class I (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name
Total Abscession FDA UDI
Generic Name
Nephrostomy catheter FDA UDI
Device Name
8F x 30cm Total Abscession Nephrostomy Drainage Catheter (Locking Pigtail) FDA UDI
Model / Reference
H787140010010 FDA UDI
Description
8F x 30cm Total Abscession Nephrostomy Drainage Catheter (Locking Pigtail) FDA UDI

Identifiers

Catalog Number
14001001 FDA UDI
Primary DI / UDI-DI
15051684011587 FDA UDI
FDA Product Code
GBO FDA UDI
GMDN Term
Nephrostomy catheter 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

Dimensions & Sizes

Size
Length — 30 Centimeter FDA UDI
Catheter Gauge — 6.5 French FDA UDI

Category: Nephrostomy catheter

Total Abscession by Angiodynamics, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nephrostomy catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiodynamics, Inc

Sources (1)

  • FDA UDI 7f19c8bf-3b12-4019-a294-c19aa7414f5b 37 fields · synced Jun 20, 2026