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Tissue Processing Unit

FDA UDI

Class I (US FDA UDI)

by InGeneron Inc.

Identity

Trade Name
Tissue Processing Unit FDA UDI
Generic Name
Stromal vascular fraction recovery unit, multi-modality FDA UDI
Model / Reference
10715-01 FDA UDI

Identifiers

Catalog Number
10715-01 FDA UDI
Primary DI / UDI-DI
00852059007109 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
Stromal vascular fraction recovery unit, multi-modality FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stromal vascular fraction recovery unit, multi-modality

Tissue Processing Unit by InGeneron Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stromal vascular fraction recovery unit, multi-modality.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
InGeneron Inc.

Sources (1)

  • FDA UDI ab411e54-fa5e-4fb1-ac3b-6d83da742636 34 fields · synced May 30, 2026