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Suction Tubes Bent - 14 Gauge -Sterile

FDA UDI

Class I (US FDA UDI)

by Adept Medical Limited

Identity

Trade Name
Suction Tubes Bent - 14 Gauge -Sterile FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Model / Reference
NZ4254Bent FDA UDI

Identifiers

Primary DI / UDI-DI
09421901970505 FDA UDI
FDA Product Code
JZF FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

No

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: Surgical/emergency suction cannula, non-illuminating, single-use

Suction Tubes Bent - 14 Gauge -Sterile by Adept Medical Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd5935ce-5083-4e89-91fa-c2521c4a7a4d 32 fields · synced Jun 6, 2026