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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
4/24/1/2SS, 4 Hook FDA UDI
Model / Reference
107-SST FDA UDI
Description
4/24/1/2SS, 4 Hook FDA UDI

Identifiers

Catalog Number
107-SST FDA UDI
Primary DI / UDI-DI
00007618875235 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
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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Pryor by Pryor Products — 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
Pryor Products

Sources (1)

  • FDA UDI d79eca01-0910-406d-b1a9-9ce2a68be23c 35 fields · synced May 30, 2026