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Adapter

FDA UDI

Class I (US FDA UDI)

by Liberty Medical Inc

Identity

Trade Name
Adapter FDA UDI
Generic Name
General-purpose brachytherapy system applicator, manual FDA UDI
Device Name
Adapter flexineedle 15ga 60mm non sterile FDA UDI
Model / Reference
7094 FDA UDI
Description
Adapter flexineedle 15ga 60mm non sterile FDA UDI

Identifiers

Primary DI / UDI-DI
B16570940326043024055 FDA UDI
FDA Product Code
IWJ FDA UDI
GMDN Term
General-purpose brachytherapy system applicator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.5650 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: General-purpose brachytherapy system applicator, manual

Adapter by Liberty Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose brachytherapy system applicator, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Liberty Medical Inc

Sources (1)

  • FDA UDI 6dbad313-f818-481c-adf5-9218fa46dbc6 33 fields · synced May 30, 2026