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ViaPeel™

FDA UDI

by Greatbatch Ltd

Identity

Trade Name
ViaPeel™ FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
PTFE Peelable Introducer FDA UDI
Model / Reference
10893-010 FDA UDI
Description
PTFE Peelable Introducer FDA UDI

Identifiers

Catalog Number
10893-010 FDA UDI
Primary DI / UDI-DI
00821329600456 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
Catheter Gauge — 7 French FDA UDI
Lumen/Inner Diameter — 2.5 Millimeter FDA UDI
Outer Diameter — .46 Millimeter FDA UDI
Length — 10 Centimeter FDA UDI

Category: Vascular catheter introduction set, nonimplantable

ViaPeel™ 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 98a3b9bb-3551-4b90-a31c-b32a40c324ca 35 fields · synced Jun 8, 2026