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Micronitinol Rapid Access Kit

FDA UDI

by Greatbatch Ltd

Identity

Trade Name
Micronitinol Rapid Access Kit FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
Micronitinol Rapid Access Coaxial Introducer Kit FDA UDI
Model / Reference
10842‐002 FDA UDI
Description
Micronitinol Rapid Access Coaxial Introducer Kit FDA UDI

Identifiers

Catalog Number
900120‐01 FDA UDI
Primary DI / UDI-DI
00821329400599 FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 9.3 Centimeter FDA UDI

Category: Vascular catheter introduction set, nonimplantable

Micronitinol Rapid Access Kit by Greatbatch Ltd — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Greatbatch Ltd

Sources (1)

  • FDA UDI 9ddc418e-2a84-47ed-ba1b-a65f2f151dd9 35 fields · synced May 30, 2026