← Back to catalogue

Hydromillex

FDA UDI

Class II (US FDA UDI)

by Merck Millipore Limited

Identity

Trade Name
Hydromillex FDA UDI
Generic Name
Haemodialysis system transducer protector FDA UDI
Model / Reference
SLST025DM FDA UDI

Identifiers

Primary DI / UDI-DI
04053252725180 FDA UDI
FDA Product Code
FIB FDA UDI
GMDN Term
Haemodialysis system transducer protector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Hydromillex by Merck Millipore Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 81bf0e77-34b2-469b-ad07-46b5c6d71835 33 fields · synced May 30, 2026