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Byrd

FDA UDI

Class I (US FDA UDI)

by Cook Vandergrift Inc.

Identity

Trade Name
Byrd FDA UDI
Generic Name
Fascial tissue dilator, single-use FDA UDI
Device Name
10.0 Fr Byrd Dilator Sheath Set (B) Extra Long Polypropylene FDA UDI
Model / Reference
G20535 FDA UDI
Description
10.0 Fr Byrd Dilator Sheath Set (B) Extra Long Polypropylene FDA UDI

Identifiers

Catalog Number
LR-PPLBES-10.0-XL FDA UDI
Primary DI / UDI-DI
00827002205352 FDA UDI
FDA Product Code
GCC FDA UDI
GMDN Term
Fascial tissue dilator, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Fascial tissue dilator, single-use

Byrd by Cook Vandergrift Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fascial tissue dilator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Vandergrift Inc.

Sources (1)

  • FDA UDI 0d78464a-b68b-4461-8edb-5afba1f2de87 36 fields · synced May 30, 2026