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1L Bottle

FDA UDI

Class I (US FDA UDI)

by Scinus Cell Expansion Netherlands B.V.

Identity

Trade Name
1L Bottle FDA UDI
Generic Name
Laboratory liquid dispenser, manual FDA UDI
Device Name
This bottle can be used for the addition and removal of liquids to/from e.g. the Adherent Bag. (single-use) FDA UDI
Model / Reference
1LB-02-01 FDA UDI
Description
This bottle can be used for the addition and removal of liquids to/from e.g. the Adherent Bag. (single-use) FDA UDI

Identifiers

Primary DI / UDI-DI
08720299213623 FDA UDI
FDA Product Code
KJF FDA UDI
GMDN Term
Laboratory liquid dispenser, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.2240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Laboratory liquid dispenser, manual

1L Bottle by Scinus Cell Expansion Netherlands B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory liquid dispenser, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Scinus Cell Expansion Netherlands B.V.

Sources (1)

  • FDA UDI 5cda73d0-c37e-411a-8095-ce8d59fa6ea7 33 fields · synced Jun 8, 2026