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Summit Medical

FDA UDI

Class I (US FDA UDI)

by Summit Medical, LLC

Identity

Trade Name
SUMMIT MEDICAL FDA UDI
Generic Name
Liposuction system cannula, reusable FDA UDI
Model / Reference
3-H-IHSL FDA UDI

Identifiers

Primary DI / UDI-DI
00385640061063 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Liposuction system cannula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system cannula, reusable

Summit Medical by Summit Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Liposuction system cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Summit Medical, LLC

Sources (1)

  • FDA UDI bf9c0494-e489-4de9-8397-9697577bd762 32 fields · synced Jun 8, 2026