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Sofia Vitalitec

FDA UDI

Class II (US FDA UDI)

by Peters Surgical

Identity

Trade Name
SOFIA VITALITEC FDA UDI
Generic Name
Surgical bulldog clamp, single-use FDA UDI
Device Name
Atraumatic Spring Clip 1/2 FORCE FDA UDI
Model / Reference
VSL-1807 FDA UDI
Description
Atraumatic Spring Clip 1/2 FORCE FDA UDI

Identifiers

Catalog Number
VSL-1807 FDA UDI
Primary DI / UDI-DI
03661522040119 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Surgical bulldog clamp, single-use 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 bulldog clamp, single-use

Sofia Vitalitec by Peters Surgical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical bulldog clamp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Peters Surgical

Sources (1)

  • FDA UDI 097ae9a8-8af4-44be-b46b-caeb254ec7f0 37 fields · synced May 31, 2026