McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name: McKesson FDA UDI
Generic Name: Finger/hand exerciser FDA UDI
Device Name: Therapy Putty xx-soft resistance level 5 lb FDA UDI
Model / Reference: 169-10-0995 FDA UDI
Description: Therapy Putty xx-soft resistance level 5 lb FDA UDI

Identifiers

Primary DI / UDI-DI: 00612479242074 FDA UDI
FDA Product Code: ION FDA UDI
IOD FDA UDI
GMDN Term: Finger/hand exerciser FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5370 FDA UDI
890.5350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Finger/hand exerciser

McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Mckesson Medical-Surgical Inc.

Sources (1)

FDA UDI 0bc6b6c0-63ef-4df0-8d25-892e53118ba7 33 fields · synced May 30, 2026