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Irrigation line 5m

FDA UDI

Class I (US FDA UDI)

by Bien-Air Surgery SA

Identity

Trade Name
Irrigation line 5m FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Model / Reference
1502152 FDA UDI

Identifiers

Catalog Number
1502152-010 FDA UDI
Primary DI / UDI-DI
17630055511000 FDA UDI
FDA Product Code
EQJ FDA UDI
HBC FDA UDI
HBE FDA UDI
NLY FDA UDI
ERL FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4140 FDA UDI
882.4360 FDA UDI
882.4310 FDA UDI
874.4250 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction/irrigation tubing, single-use

Irrigation line 5m by Bien-Air Surgery SA — Class I — 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

Manufacturer
Bien-Air Surgery SA

Sources (1)

  • FDA UDI 9d8fcc63-0745-4d44-81e4-70ace2fa0e6c 33 fields · synced Jun 6, 2026