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Span-America

FDA UDI

Class I (US FDA UDI)

by Span-America Medical Systems, Inc.

Identity

Trade Name
Span-America FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
GEO LAM POS RPLCMT STRIP 6ST/C (P01408) FDA UDI
Model / Reference
SPAN AIDS FDA UDI
Description
GEO LAM POS RPLCMT STRIP 6ST/C (P01408) FDA UDI

Identifiers

Catalog Number
SP418-000 FDA UDI
Primary DI / UDI-DI
H933SP418000 FDA UDI
FDA Product Code
KIC FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3175 FDA UDI
Commercial Distribution
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

Category: Freestanding patient positioner, single-use

Span-America by Span-America Medical Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4c45e2d5-adb1-4bfb-9724-03a5b03e48f5 34 fields · synced Jun 12, 2026