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Purist

FDA UDI

Class I (US FDA UDI)

by Adsm

Identity

Trade Name
PURIST FDA UDI
Generic Name
Operating table orthopaedic extension, non-powered FDA UDI
Device Name
Leg Positioning System FDA UDI
Model / Reference
6813100 FDA UDI
Description
Leg Positioning System FDA UDI

Identifiers

Catalog Number
6813100 FDA UDI
Primary DI / UDI-DI
03701091005352 FDA UDI
FDA Product Code
BWN FDA UDI
GMDN Term
Operating table orthopaedic extension, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 FDA UDI
Commercial Distribution
Not 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

Yes

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
MRI Safety
MR Safe FDA UDI

Purist by Adsm — 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

Manufacturer
Adsm

Sources (1)

  • FDA UDI 6fae2228-b142-460c-9a08-3eb3e37890ae 36 fields · synced May 31, 2026