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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 TUBE, 6' (1.8M) X 1/4" (6.35MM) DEPH FREE FDA UDI
Model / Reference
536010DF50 FDA UDI
Description
SUCTION TUBE, 6' (1.8M) X 1/4" (6.35MM) DEPH FREE FDA UDI

Identifiers

Catalog Number
536010DF50 FDA UDI
Primary DI / UDI-DI
10073088151916 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
Not 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 — 6 Feet FDA UDI

Bemis by Bemis Manufacturing Co. — Class II — 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 ae73e806-01aa-40a1-8872-f53266a22f53 36 fields · synced May 30, 2026