← Back to catalogue

Reprocessed Universal Cannula Set Without Fenestration

FDA UDI

Class I (US FDA UDI)

by Suretek Medical

Identity

Trade Name
Reprocessed Universal Cannula Set Without Fenestration FDA UDI
Generic Name
Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use FDA UDI
Device Name
5.5mm (I.D.) X 70mm FDA UDI
Model / Reference
9718 FDA UDI
Description
5.5mm (I.D.) X 70mm FDA UDI

Identifiers

Primary DI / UDI-DI
B39097181 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use

Reprocessed Universal Cannula Set Without Fenestration by Suretek Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological concentrate/haemostatic agent applicator cannula, endoscopic, single-use.

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

Manufacturer
Suretek Medical

Sources (1)

  • FDA UDI 0272414b-2664-4f84-b2db-307cfa2b630d 33 fields · synced May 31, 2026