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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 drainage kit FDA UDI
Device Name
ReliaVac 100 Closed Wound Suction Kit, Medium Suction, 100cc Evacuator, Y-Connecting Tube, Silicone Round Drain, Medium 1/8", (3.2mm) O.D., 10"(25.4cm) Hole Pattern, X-Ray Opaque Stripe, Attached Trocar FDA UDI
Model / Reference
0085310 FDA UDI
Description
ReliaVac 100 Closed Wound Suction Kit, Medium Suction, 100cc Evacuator, Y-Connecting Tube, Silicone Round Drain, Medium 1/8", (3.2mm) O.D., 10"(25.4cm) Hole Pattern, X-Ray Opaque Stripe, Attached Trocar FDA UDI

Identifiers

Catalog Number
0085310 FDA UDI
Primary DI / UDI-DI
00801741050152 FDA UDI
FDA Product Code
GCY FDA UDI
GMDN Term
Closed-wound drainage kit 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

Yes

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
Outer Diameter — 3.2 Millimeter FDA UDI

Category: Closed-wound drainage kit

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 drainage kit.

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 6e3fb109-ea51-46fc-8204-ea1e278745f8 36 fields · synced Jun 1, 2026