← Back to catalogue

Sherpa Nx Balanced

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
SHERPA NX BALANCED FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
CATHETER SB7AL20 SB 7F 100CM AL20 FDA UDI
Model / Reference
SB7AL20 FDA UDI
Description
CATHETER SB7AL20 SB 7F 100CM AL20 FDA UDI

Identifiers

Primary DI / UDI-DI
00613994836779 FDA UDI
510(k) Number
K051846 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Dimensions & Sizes

Size
Catheter Gauge — 7.0 French FDA UDI
Length — 100.0 Centimeter FDA UDI

Category: Vascular guide-catheter, single-use

Sherpa Nx Balanced by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

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 109b4313-6c32-4a24-8078-8b902324f069 37 fields · synced Jun 6, 2026