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Pedigo Products, Inc.

FDA UDI

Class II (US FDA UDI)

by Pedigo Products, Inc.

Identity

Trade Name
Pedigo Products, Inc. FDA UDI
Generic Name
Hospital stretcher, manual FDA UDI
Device Name
7500-NE: Eye Stretcher, narrow. With hydraulic height adjustment, pneumatic adjustable Fowler, Recovery Knee Gatch, Quick-Release FDA UDI
Model / Reference
7500-NE FDA UDI
Description
7500-NE: Eye Stretcher, narrow. With hydraulic height adjustment, pneumatic adjustable Fowler, Recovery Knee Gatch, Quick-Release FDA UDI

Identifiers

Catalog Number
7500-NE FDA UDI
Primary DI / UDI-DI
00841027100263 FDA UDI
FDA Product Code
FPO FDA UDI
GMDN Term
Hospital stretcher, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6910 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Pedigo Products, Inc. by Pedigo Products, Inc. — Class II — 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

Sources (1)

  • FDA UDI b6cffbd7-2a11-40a0-a386-c0043f64a04f 36 fields · synced Jun 8, 2026