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Life Instruments

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 798-0507-1

by Life Instrument Corporation

Identity

Trade Name
Suction Tube EUDAMED
Life Instruments FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI
Device Name
Suction Tubes EUDAMED
Stainless Frazier Suction 7FR 4.5" from bend FDA UDI
Model / Reference
798-0507-1 EUDAMEDFDA UDI
Description
Stainless Frazier Suction 7FR 4.5" from bend FDA UDI

Identifiers

Primary DI / UDI-DI
M930798050710 EUDAMEDFDA UDI
Basic UDI-DI
++M930009QB EUDAMED
FDA Product Code
MDM FDA UDI
EMDN Code
L030101 SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE EUDAMED
GMDN Term
Surgical/emergency suction cannula, non-illuminating, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Life Instruments by Life Instrument Corporation — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI d32c552d-bfa2-4e9d-8660-15db8d80c7c7 33 fields · synced Oct 6, 2026
  • EUDAMED a3013e75-3430-451e-ad9a-52c72d3c6bd5 61 fields · synced Oct 6, 2026