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Touch Micro-OSMETTE Probe

FDA UDI

Class I (US FDA UDI)

by Precision Systems, Inc.

Identity

Trade Name
Touch Micro-OSMETTE Probe FDA UDI
Generic Name
Osmolality IVD, kit, freezing point FDA UDI
Device Name
Touch Micro-OSMETTE Probe FDA UDI
Model / Reference
2013 FDA UDI
Description
Touch Micro-OSMETTE Probe FDA UDI

Identifiers

Catalog Number
2013 FDA UDI
Primary DI / UDI-DI
00850041049519 FDA UDI
FDA Product Code
JJM FDA UDI
GMDN Term
Osmolality IVD, kit, freezing point FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2730 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Osmolality IVD, kit, freezing point

Touch Micro-OSMETTE Probe by Precision Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Osmolality IVD, kit, freezing point.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 09cc6ac3-2579-4439-b31d-34d1c6934e41 35 fields · synced May 30, 2026