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Lid 1

FDA UDI

Class I (US FDA UDI)

by Bradshaw Medical Inc.

Identity

Trade Name
LID 1 FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
The lid is designed to fit securely over the base, creating a sealed environment. It features a filter system, typically a perforated plate with a disposable filter, that allows sterilizing agents (like steam or gas) to enter the container and reach the instruments. After the sterilization cycle is complete, this filter system prevents microorganisms from entering, thereby maintaining the sterility of the contents until the container is opened for use. FDA UDI
Model / Reference
MRS-116-01-01 FDA UDI
Description
The lid is designed to fit securely over the base, creating a sealed environment. It features a filter system, typically a perforated plate with a disposable filter, that allows sterilizing agents (like steam or gas) to enter the container and reach the instruments. After the sterilization cycle is complete, this filter system prevents microorganisms from entering, thereby maintaining the sterility of the contents until the container is opened for use. FDA UDI

Identifiers

Primary DI / UDI-DI
00810019931895 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

Lid 1 by Bradshaw Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9cdc9c98-cbf7-4ba7-bcc1-3ef6a5fa0d0c 33 fields · synced May 30, 2026