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Transparent Disp. Tube Tolders (for HemataSTAT +2 more)

FDA UDI

Class II (US FDA UDI)

by Separation Technology, Inc.

Identity

Trade Name
Transparent Disp. Tube Tolders (for HemataSTAT, Cream 50/pkg) FDA UDI
Generic Name
Centrifuge bucket/tube holder adaptor FDA UDI
Model / Reference
230-100 FDA UDI

Identifiers

Catalog Number
230-100 FDA UDI
Primary DI / UDI-DI
00831829000229 FDA UDI
FDA Product Code
GKG FDA UDI
GMDN Term
Centrifuge bucket/tube holder adaptor FDA UDI
Models / Variants
for HemataSTAT FDA UDI
Cream 50 FDA UDI
pkg FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6400 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Centrifuge bucket/tube holder adaptor

Transparent Disp. Tube Tolders (for HemataSTAT +2 more) by Separation Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — 3 models

Similar devices

Also classified as Centrifuge bucket/tube holder adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Separation Technology, Inc.

Sources (1)

  • FDA UDI 82c0b5a1-c7c0-416f-9bf1-5409cbf7e4b4 34 fields · synced May 30, 2026