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FCP Bandage

FDA UDI

Class I (US FDA UDI)

by First Care Products Ltd

Identity

Trade Name
FCP Bandage FDA UDI
Generic Name
Abdominal paracentesis needle, reprocessed FDA UDI
Device Name
WS-05 – 4" WoundStop Care1 FDA UDI
Model / Reference
WoundStop Care1 FDA UDI
Description
WS-05 – 4" WoundStop Care1 FDA UDI

Identifiers

Catalog Number
WS-05 FDA UDI
Primary DI / UDI-DI
07290017050157 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Abdominal paracentesis needle, reprocessed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Abdominal paracentesis needle, reprocessed

FCP Bandage by First Care Products Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal paracentesis needle, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1abed482-1616-47e0-9537-286d463f825e 35 fields · synced May 30, 2026