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Powder Coated Grab Bar 12"

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Powder Coated Grab Bar 12" FDA UDI
Generic Name
Parallel bar exerciser, non-powered FDA UDI
Model / Reference
10305 FDA UDI

Identifiers

Primary DI / UDI-DI
00616784030517 FDA UDI
FDA Product Code
ILS FDA UDI
GMDN Term
Parallel bar exerciser, non-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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: Parallel bar exerciser, non-powered

Powder Coated Grab Bar 12" by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Parallel bar exerciser, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI e99811c4-cac9-4abd-a68a-d91010c4a850 32 fields · synced Jun 6, 2026