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Ent Mr8

FDA UDI

Class II (US FDA UDI)

by Medtronic Powered Surgical Solutions

Identity

Trade Name
ENT MR8 FDA UDI
Generic Name
Medical device integration rack FDA UDI
Device Name
RACK 1847BRACK ENTMR8 BUR RACK FDA UDI
Model / Reference
1847BRACK FDA UDI
Description
RACK 1847BRACK ENTMR8 BUR RACK FDA UDI

Identifiers

Primary DI / UDI-DI
00763000357023 FDA UDI
510(k) Number
K183515 FDA UDI
FDA Product Code
ERL FDA UDI
GMDN Term
Medical device integration rack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4250 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Medical device integration rack

Ent Mr8 by Medtronic Powered Surgical Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device integration rack.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1073e956-30dc-49b0-8680-422955bacb6d 35 fields · synced Jun 9, 2026