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Flexi-Lock Tubing Limb 0.7m to 2.0m 22mm Tube with 2 x 22mm F Serrated Connector

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
Flexi-Lock Tubing Limb 0.7m to 2.0m 22mm Tube with 2 x 22mm F Serrated Connector FDA UDI
Generic Name
Inspiratory/expiratory limb respiratory tubing, single-use FDA UDI
Model / Reference
038-01-241U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788749097 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Inspiratory/expiratory limb respiratory tubing, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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: Inspiratory/expiratory limb respiratory tubing, single-use

Flexi-Lock Tubing Limb 0.7m to 2.0m 22mm Tube with 2 x 22mm F Serrated Connector by Flexicare Medical Limited — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Inspiratory/expiratory limb respiratory tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flexicare Medical Limited

Sources (1)

  • FDA UDI 8f223ebc-2351-4f44-9a62-9182e9962dc8 32 fields · synced Jun 8, 2026