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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
Torso Pad 20" x 24" x 1" w/ Elastak (one side) FDA UDI
Model / Reference
20" x 24" Torso Pad (one side) FDA UDI
Description
Torso Pad 20" x 24" x 1" w/ Elastak (one side) FDA UDI

Identifiers

Catalog Number
SLFP1E2024 FDA UDI
Primary DI / UDI-DI
00850047863287 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
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f1f4824-081a-4ea1-ad70-549596a86c56 36 fields · synced May 30, 2026