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Bard® Parsonnet Pulse Generator Pouches

FDA UDI

Class I (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
Bard® Parsonnet Pulse Generator Pouches FDA UDI
Generic Name
Implantable pulse generator mesh bag, non-bioabsorbable FDA UDI
Device Name
Bard® Parsonnet Pulse Generator Pouch, X-Large FDA UDI
Model / Reference
002906 FDA UDI
Description
Bard® Parsonnet Pulse Generator Pouch, X-Large FDA UDI

Identifiers

Catalog Number
002906 FDA UDI
Primary DI / UDI-DI
00801741040979 FDA UDI
FDA Product Code
DSW FDA UDI
GMDN Term
Implantable pulse generator mesh bag, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.3650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Implantable pulse generator mesh bag, non-bioabsorbable

Bard® Parsonnet Pulse Generator Pouches by Bard Peripheral Vascular — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable pulse generator mesh bag, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Peripheral Vascular

Sources (1)

  • FDA UDI baef36db-d7e4-4fe4-be33-c87a47761b7c 36 fields · synced May 30, 2026