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Busse Hospital Disposables

FDA UDI

Class I (US FDA UDI)

by Robert Busse & Co., Inc.

Identity

Trade Name
Busse Hospital Disposables FDA UDI
Generic Name
Low-pressure tubing connector, single-use, sterile FDA UDI
Device Name
'Y" Connector FDA UDI
Model / Reference
508 FDA UDI
Description
'Y" Connector FDA UDI

Identifiers

Catalog Number
508 FDA UDI
Primary DI / UDI-DI
00849233012486 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Low-pressure tubing connector, single-use, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

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: Low-pressure tubing connector, single-use, sterile

Busse Hospital Disposables by Robert Busse & Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Low-pressure tubing connector, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8db911f4-56ab-4bf6-97d0-b0cb03ee7013 34 fields · synced May 30, 2026