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Disconnect Wedge

FDA UDI

Class I (US FDA UDI)

by Mercury Enterprises, Inc.

Identity

Trade Name
Disconnect Wedge FDA UDI
Generic Name
Respiratory connector disconnection wedge FDA UDI
Model / Reference
10-55340 FDA UDI

Identifiers

Primary DI / UDI-DI
10641043553404 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Respiratory connector disconnection wedge 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Category: Respiratory connector disconnection wedge

Disconnect Wedge by Mercury Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1ab3d895-a4b0-45f4-a443-540548eb2a68 33 fields · synced May 30, 2026