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Pose Health Care Limited

FDA UDI

Class I (US FDA UDI)

by Pose Health Care Limited

Identity

Trade Name
POSE HEALTH CARE LIMITED FDA UDI
Generic Name
Instrument rinsing agent FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
08859335502220 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Instrument rinsing agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Instrument rinsing agent

Pose Health Care Limited by Pose Health Care Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument rinsing agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2163c53e-fec4-42eb-9835-693e59ec6b36 32 fields · synced May 30, 2026