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Evacuator

FDA UDI

Class I (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Evacuator FDA UDI
Generic Name
Closed-wound drainage kit FDA UDI
Device Name
ReliaVac 400 Evacuator, 400cc Evacuator, 35" (88.9cm) Y-Connecting Tube FDA UDI
Model / Reference
0070800 FDA UDI
Description
ReliaVac 400 Evacuator, 400cc Evacuator, 35" (88.9cm) Y-Connecting Tube FDA UDI

Identifiers

Catalog Number
0070800 FDA UDI
Primary DI / UDI-DI
00801741049606 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

Yes

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
Total Volume — 400 Milliliter FDA UDI
Length — 35 Inch FDA UDI

Category: Closed-wound drainage kit

Evacuator 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 c80ba225-50e0-402b-bbfd-9e08c97890af 36 fields · synced May 30, 2026