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Degania

FDA UDI

Class II (US FDA UDI)

by Degania Silicone Ltd

Identity

Trade Name
Degania FDA UDI
Generic Name
Surgical vessel loop FDA UDI
Device Name
Identi Loops Maxi Red 18" sterile FDA UDI
Model / Reference
231151080DS FDA UDI
Description
Identi Loops Maxi Red 18" sterile FDA UDI

Identifiers

Primary DI / UDI-DI
07290001603079 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical vessel loop FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical vessel loop

Degania by Degania Silicone Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical vessel loop.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 864c3bed-64a1-44db-806f-0bf5b8eed319 33 fields · synced Jun 8, 2026