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SurgiLock

FDA UDI

Class I (US FDA UDI)

by Medicalock Corporation

Identity

Trade Name
SurgiLock FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
Standard Head Positioner w/ Elastak 20" x 24" Torso Pad w/ Elastak (2) Jelly Wrap w/ Elastak FDA UDI
Model / Reference
Robotics Positioning Kit FDA UDI
Description
Standard Head Positioner w/ Elastak 20" x 24" Torso Pad w/ Elastak (2) Jelly Wrap w/ Elastak FDA UDI

Identifiers

Catalog Number
SLFSHTPJWK FDA UDI
Primary DI / UDI-DI
00850047863454 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Freestanding patient positioner, single-use

SurgiLock by Medicalock Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 903b76b5-bcb4-4a04-96c0-befba35de9b9 35 fields · synced Jun 6, 2026