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MD Resource

FDA UDI

Class II (US FDA UDI)

by Medical Device Resource Corp.

Identity

Trade Name
MD Resource FDA UDI
Generic Name
Surgical suction system FDA UDI
Device Name
RM2000 Aspirator FDA UDI
Model / Reference
RM2000 FDA UDI
Description
RM2000 Aspirator FDA UDI

Identifiers

Catalog Number
RM2000 FDA UDI
Primary DI / UDI-DI
00859898006454 FDA UDI
510(k) Number
K850704 FDA UDI
FDA Product Code
JCX FDA UDI
GMDN Term
Surgical suction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical suction system

MD Resource by Medical Device Resource Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cb5a686f-45d2-4f51-a9f3-3cea17358d38 36 fields · synced Jun 8, 2026