← Back to catalogue

Cradle

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 642-511

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
Cradle EUDAMEDFDA UDI
Generic Name
Prostate brachytherapy system applicator, manual FDA UDI
Device Name
AccuCARE Equipment & Template Grids – (Classic Steppers) EUDAMED
For use with GE E7C8L Classic Steppers FDA UDI
Model / Reference
642-511 EUDAMEDFDA UDI
Description
For use with GE E7C8L Classic Steppers FDA UDI

Identifiers

Catalog Number
642-511 FDA UDI
Primary DI / UDI-DI
00841436121095 EUDAMEDFDA UDI
Basic UDI-DI
0841436101TD301B1NY EUDAMED
510(k) Number
K131161 FDA UDI
FDA Product Code
ITX FDA UDI
EMDN Code
Z11010380 BRACHYTHERAPY RADIATION SYSTEMS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Prostate brachytherapy system applicator, manual FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Category: Prostate brachytherapy system applicator, manual

Cradle by Civco Medical Instruments Co., Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Prostate brachytherapy system applicator, manual.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI fccf4a32-b089-4afa-a34a-8ff865bfc0ac 36 fields · synced Aug 3, 2026
  • EUDAMED 4ce943dc-f54e-4c83-a930-743f07d6a9f5 61 fields · synced Aug 3, 2026