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OncoSeedTM

FDA UDI

Class II (US FDA UDI)

by Medi-Physics, Inc.

Identity

Trade Name
OncoSeedTM FDA UDI
Generic Name
Manual brachytherapy source, permanent implant FDA UDI
Model / Reference
6711 - Iodine I-125 Seed 17.70 mCi FDA UDI

Identifiers

Catalog Number
6711-17700 FDA UDI
Primary DI / UDI-DI
00840682100632 FDA UDI
FDA Product Code
KXK FDA UDI
GMDN Term
Manual brachytherapy source, permanent implant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual brachytherapy source, permanent implant

OncoSeedTM by Medi-Physics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual brachytherapy source, permanent implant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medi-Physics, Inc.

Sources (1)

  • FDA UDI 4445a507-15ea-4eb1-bb18-0e9008de7d71 34 fields · synced Jun 1, 2026