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ReverseTM

FDA UDI

Class II (US FDA UDI)

by Reverse Medical Corporation

Identity

Trade Name
ReverseTM FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
MIC-027-150 REVERSE MICROCATHETER FDA UDI
Model / Reference
MIC-027-150 FDA UDI
Description
MIC-027-150 REVERSE MICROCATHETER FDA UDI

Identifiers

Primary DI / UDI-DI
00847536003569 FDA UDI
510(k) Number
K130858 FDA UDI
FDA Product Code
DQO FDA UDI
KRA FDA UDI
DQY FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 FDA UDI
870.1210 FDA UDI
870.1250 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

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

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Vascular guide-catheter, single-use

ReverseTM by Reverse Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular guide-catheter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reverse Medical Corporation

Sources (1)

  • FDA UDI 79b6cd30-3ecc-4594-b783-5a8e2d13e922 36 fields · synced May 30, 2026