Wateer Trap(screw Cap)

FDA UDI

Class I (US FDA UDI)

by Besmed Health Business Corp.

Identity

Trade Name: WATEER TRAP(SCREW CAP) FDA UDI
Generic Name: Breathing circuit condensate trap, single-use FDA UDI
Device Name: WATEER TRAP(SCREW CAP) FDA UDI
Model / Reference: WT-96131 FDA UDI
Description: WATEER TRAP(SCREW CAP) FDA UDI

Identifiers

Primary DI / UDI-DI: 04716770961316 FDA UDI
FDA Product Code: BYX FDA UDI
GMDN Term: Breathing circuit condensate trap, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breathing circuit condensate trap, single-use

Wateer Trap(screw Cap) by Besmed Health Business Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Besmed Health Business Corp.

Sources (1)

FDA UDI 5d2964d4-377f-4450-9332-7218b1ac7700 33 fields · synced May 30, 2026