Cervos Lipo Pro Double Pack

FDA UDI

Class II (US FDA UDI)

by Ranfac Corp.

Identity

Trade Name: Cervos Lipo Pro Double Pack FDA UDI
Generic Name: Autologous adipose tissue reinjection set FDA UDI
Device Name: CER-LP PROCESS DISPOSABLE PACK PN: 69001-01M FDA UDI
Model / Reference: CER-LP-40 FDA UDI
Description: CER-LP PROCESS DISPOSABLE PACK PN: 69001-01M FDA UDI

Identifiers

Catalog Number: CER-LP-40 FDA UDI
Primary DI / UDI-DI: 00850023741578 FDA UDI
510(k) Number: K150156 FDA UDI
FDA Product Code: MUU FDA UDI
GMDN Term: Autologous adipose tissue reinjection set FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.5040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Total Volume — 40 Milliliter FDA UDI

Category: Autologous adipose tissue reinjection set

Cervos Lipo Pro Double Pack by Ranfac Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Autologous adipose tissue reinjection set.

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Adinizer — Bsl Co. · Class II
Disposable cannula 2.0mm X 20cm long, 6 spiral slots — Millennium Medical Technologies, Inc. · Class I
Adinizer — Bsl Co. · Class II
Adinizer — Bsl Co. · Class II

Cleared under the same submission

K150156 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Ranfac Corp.

Sources (1)

FDA UDI 8bdb58db-2f52-4293-bcfc-230104e4e8b5 38 fields · synced Jun 1, 2026