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Closed Wound Suction

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Closed Wound Suction FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Device Name
100cc Silicone Closed Wound Suction Evacuator Kit, 100cc Silicone Evacuator with Anti-Reflux Valve, Hubless Silicone Flat Drain 10mm Wide, 20cm Long, Fully Perforated Drain with Trocar, X-Ray Opaque FDA UDI
Model / Reference
0072440 FDA UDI
Description
100cc Silicone Closed Wound Suction Evacuator Kit, 100cc Silicone Evacuator with Anti-Reflux Valve, Hubless Silicone Flat Drain 10mm Wide, 20cm Long, Fully Perforated Drain with Trocar, X-Ray Opaque FDA UDI

Identifiers

Catalog Number
0072440 FDA UDI
Primary DI / UDI-DI
00801741050039 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Closed-wound drain, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 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

Yes

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
Width — 10 Millimeter FDA UDI

Category: Closed-wound drain, non-bioabsorbable

Closed Wound Suction by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drain, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 1cff95a6-1cd2-4de0-bd43-642e445a236e 36 fields · synced Jun 8, 2026