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G.E.B. tubing

FDA UDI

Class II (US FDA UDI)

by A1 Surgical Supplies, Llc

Identity

Trade Name
G.E.B. tubing FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
Suction tube FDA UDI
Model / Reference
1 FDA UDI
Description
Suction tube FDA UDI

Identifiers

Primary DI / UDI-DI
10860000082812 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Suction/irrigation tubing, single-use

G.E.B. tubing by A1 Surgical Supplies, Llc — 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 7dad742f-113b-4489-994b-294edecd9130 33 fields · synced Jun 6, 2026