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SOMAVAC 100 Vacuum Source

FDA UDI

Class I (US FDA UDI)

by Somavac Medical Solutions, Inc.

Identity

Trade Name
SOMAVAC 100 Vacuum Source FDA UDI
Generic Name
Closed-wound drainage suction pump FDA UDI
Device Name
Portable battery powered vacuum source at 100mmHg FDA UDI
Model / Reference
20011 FDA UDI
Description
Portable battery powered vacuum source at 100mmHg FDA UDI

Identifiers

Catalog Number
20011 FDA UDI
Primary DI / UDI-DI
00850004219010 FDA UDI
FDA Product Code
GCY FDA UDI
BTA FDA UDI
GMDN Term
Closed-wound drainage suction pump FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4680 FDA UDI
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Closed-wound drainage suction pump

SOMAVAC 100 Vacuum Source by Somavac Medical Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drainage suction pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Somavac Medical Solutions, Inc.

Sources (1)

  • FDA UDI 746c08bf-c8cc-4a6f-a976-27e464a17a45 34 fields · synced May 29, 2026