← Back to catalogue

Bird

FDA UDI

Class II (US FDA UDI)

by Gaylord Solutions, LLC

Identity

Trade Name
BIRD FDA UDI
Generic Name
General-purpose surgical suction system, vacuum FDA UDI
Device Name
Breast Implant Removal Device, 2 Pack FDA UDI
Model / Reference
EMD0003 FDA UDI
Description
Breast Implant Removal Device, 2 Pack FDA UDI

Identifiers

Catalog Number
EMD0003 FDA UDI
Primary DI / UDI-DI
00860011750215 FDA UDI
510(k) Number
DEN220082 FDA UDI
FDA Product Code
QVS FDA UDI
GMDN Term
General-purpose surgical suction system, vacuum FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4675 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: General-purpose surgical suction system, vacuum

Bird by Gaylord Solutions, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical suction system, vacuum.

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
Gaylord Solutions, LLC

Sources (1)

  • FDA UDI 936080e1-942f-4bfb-8a38-30c9ec0eb883 35 fields · synced May 29, 2026