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Marker Seed - Preloaded in PSS1820SL3 Round Hub Needles, 3pk

FDA UDI

Class I (US FDA UDI)

by Eckert & Ziegler BEBIG GmbH

Identity

Trade Name
Marker Seed - Preloaded in PSS1820SL3 Round Hub Needles, 3pk FDA UDI
Generic Name
Manual brachytherapy system FDA UDI
Model / Reference
PSS1820SL3 Round Hub Needles, 3pk FDA UDI

Identifiers

Catalog Number
MO845SL3-3 FDA UDI
Primary DI / UDI-DI
00815165020424 FDA UDI
FDA Product Code
IWJ FDA UDI
GMDN Term
Manual brachytherapy system 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Brachytherapy source spacerManual brachytherapy system

Marker Seed - Preloaded in PSS1820SL3 Round Hub Needles, 3pk by Eckert & Ziegler BEBIG GmbH — Class I — 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 e8c37e56-cd1a-4d5f-8c66-ac247bc26139 34 fields · synced Jun 6, 2026