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AnchorSeed Brachytherapy Kit I125 - Preloaded magazines in sterile packagin

FDA UDI

by Eckert & Ziegler BEBIG GmbH

Identity

Trade Name
AnchorSeed Brachytherapy Kit I125 - Preloaded magazines in sterile packagin FDA UDI
Generic Name
Manual brachytherapy system FDA UDI
Model / Reference
AnchorSeed Brachytherapy Kit I125 - Preloaded magazines in sterile packagin FDA UDI

Identifiers

Catalog Number
ASKITI125 FDA UDI
Primary DI / UDI-DI
00815165020073 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

No

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

AnchorSeed Brachytherapy Kit I125 - Preloaded magazines in sterile packagin by Eckert & Ziegler BEBIG GmbH — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Manual brachytherapy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 241c44eb-6aa7-4b92-bbca-e5b9ad46471e 34 fields · synced May 30, 2026