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Slide Block

FDA UDI

Class I (US FDA UDI)

by Signal Medical Corp.

Identity

Trade Name
Slide Block FDA UDI
Generic Name
Leg procedure positioner FDA UDI
Device Name
Knee Positioner Slide Block FDA UDI
Model / Reference
BIO-1-1021 FDA UDI
Description
Knee Positioner Slide Block FDA UDI

Identifiers

Catalog Number
BIO-1-1021 FDA UDI
Primary DI / UDI-DI
B046BIO110210 FDA UDI
FDA Product Code
JEB FDA UDI
GMDN Term
Leg procedure positioner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

No

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: Leg procedure positioner

Slide Block by Signal Medical Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Leg procedure positioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22b32d3b-c1fc-4455-8faa-23e9d1bc2abd 35 fields · synced May 30, 2026