← Back to catalogue

Weck

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
WECK FDA UDI
Generic Name
Suction cannula, single-use FDA UDI
Device Name
COAGULATION SUCTION TUBE, DISPOSABLE, WITH STYLET, 8", 10/BX FDA UDI
Model / Reference
IPN010077 FDA UDI
Description
COAGULATION SUCTION TUBE, DISPOSABLE, WITH STYLET, 8", 10/BX FDA UDI

Identifiers

Catalog Number
809610 FDA UDI
Primary DI / UDI-DI
04026704601561 FDA UDI
510(k) Number
K881413 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Suction cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 20.5 Centimeter FDA UDI

Category: Suction cannula, single-use

Weck by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction cannula, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI dfa49dd3-9dae-4acb-b02c-902d90b43b86 37 fields · synced May 30, 2026