← Back to catalogue

AnchorLoad Brachytherapy Kit

FDA UDI

by Eckert & Ziegler BEBIG GmbH

Identity

Trade Name
AnchorLoad Brachytherapy Kit FDA UDI
Generic Name
Manual brachytherapy system FDA UDI
Model / Reference
AnchorLoad Brachytherapy Kit FDA UDI

Identifiers

Catalog Number
ALKIT FDA UDI
Primary DI / UDI-DI
00815165020004 FDA UDI
GMDN Term
Manual brachytherapy system FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual brachytherapy system

AnchorLoad Brachytherapy Kit by Eckert & Ziegler BEBIG GmbH — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual brachytherapy system.

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 59578470-adf8-41d7-a40c-f49357d3b9c3 34 fields · synced May 30, 2026