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Shielding Segment 180°

FDA UDI

Class II (US FDA UDI)

by Eckert & Ziegler BEBIG GmbH

Identity

Trade Name
Shielding Segment 180° FDA UDI
Generic Name
Vaginal brachytherapy system applicator, remote-afterloading FDA UDI
Model / Reference
LA320-180#02 FDA UDI

Identifiers

Catalog Number
LA320-180 FDA UDI
Primary DI / UDI-DI
04049223107413 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
Vaginal brachytherapy system applicator, remote-afterloading FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5700 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Shielding Segment 180° by Eckert & Ziegler BEBIG GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eckert & Ziegler BEBIG GmbH

Sources (1)

  • FDA UDI daf76e76-7c4d-4335-9b16-8adaf57528c2 35 fields · synced May 30, 2026