← Back to catalogue

SurgiLock

FDA UDI

Class II (US FDA UDI)

by Medicalock Corporation

Identity

Trade Name
SurgiLock FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Instrument Platform, 10" X 16", Sterile FDA UDI
Model / Reference
SL1016 FDA UDI
Description
Instrument Platform, 10" X 16", Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00850047863003 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General surgical procedure kit, non-medicated, single-use

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

Similar devices

Also classified as General surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Medicalock Corporation

Sources (1)

  • FDA UDI e6c2a84c-8097-4630-b0cb-03c3f25de430 35 fields · synced Jun 8, 2026