← Back to catalogue

Everest™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
EVEREST™ FDA UDI
Generic Name
Catheter/overtube balloon inflator, single-use FDA UDI
Device Name
SURVIVAL KIT AC3205P EVEREST 30 TJM FDA UDI
Model / Reference
AC3205P FDA UDI
Description
SURVIVAL KIT AC3205P EVEREST 30 TJM FDA UDI

Identifiers

Primary DI / UDI-DI
00643169014817 FDA UDI
510(k) Number
K960983 FDA UDI
FDA Product Code
MAV FDA UDI
GMDN Term
Catheter/overtube balloon inflator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

Yes

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

Category: Catheter/overtube balloon inflator, single-use

Everest™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Catheter/overtube balloon inflator, single-use.

Cleared under the same submission

K960983 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI f761a988-3b79-4993-b6a5-576e93e555ef 37 fields · synced Jun 8, 2026