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Pryor

FDA UDI

Class I (US FDA UDI)

by Pryor Products

Identity

Trade Name
Pryor FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
5 leg knockdown,5 hook, SW FDA UDI
Model / Reference
136T FDA UDI
Description
5 leg knockdown,5 hook, SW FDA UDI

Identifiers

Catalog Number
136T FDA UDI
Primary DI / UDI-DI
00761887000957 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Freestanding/bed-attached intravenous pole FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 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

Yes

FDA UDI

Category: Freestanding/bed-attached intravenous pole

Pryor by Pryor Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding/bed-attached intravenous pole.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pryor Products

Sources (1)

  • FDA UDI bd3439db-ca51-4679-977f-5fb4052d1bb4 34 fields · synced May 30, 2026