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Bemis

FDA UDI

Class II (US FDA UDI)

by Bemis Manufacturing Co.

Identity

Trade Name
Bemis FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
SUCTION CONNECTING TUBE, 18" (457MM) LONG X 1/4" (6.35MM) I.D. FDA UDI
Model / Reference
536510 FDA UDI
Description
SUCTION CONNECTING TUBE, 18" (457MM) LONG X 1/4" (6.35MM) I.D. FDA UDI

Identifiers

Catalog Number
536510 FDA UDI
Primary DI / UDI-DI
10073088150445 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Length — 18 Inch FDA UDI

Category: Suction/irrigation tubing, single-use

Bemis by Bemis Manufacturing Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 683b5bb9-b6af-40e2-bdd0-fff656295fc8 35 fields · synced Jun 1, 2026