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Aed-Slt Medtronic-Stop

FDA UDI

Class I (US FDA UDI)

by National Advanced Endoscopy Devices, Inc.

Identity

Trade Name
AED-SLT MEDTRONIC-STOP FDA UDI
Generic Name
Surgical power tool maintenance unit FDA UDI
Device Name
A hermetic seal tester for a Medtronic medical power tool FDA UDI
Model / Reference
SLT-MED FDA UDI
Description
A hermetic seal tester for a Medtronic medical power tool FDA UDI

Identifiers

Catalog Number
SLT-MED FDA UDI
Primary DI / UDI-DI
00848657074957 FDA UDI
FDA Product Code
GEY FDA UDI
GMDN Term
Surgical power tool maintenance unit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical power tool maintenance unit

Aed-Slt Medtronic-Stop by National Advanced Endoscopy Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool maintenance unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8518d9b5-613a-4efe-9f34-5ca70d880752 35 fields · synced May 30, 2026