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Tub Rail: Plastic

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Tub Rail: Plastic FDA UDI
Generic Name
Bath hand rail FDA UDI
Model / Reference
10341 FDA UDI

Identifiers

Primary DI / UDI-DI
00616784034119 FDA UDI
FDA Product Code
ILS FDA UDI
GMDN Term
Bath hand rail 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

Yes

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: Bath hand rail

Tub Rail: Plastic by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bath hand rail.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 5be18550-709b-4fe3-8643-ab501f274630 32 fields · synced May 29, 2026