← Back to catalogue

Schwartz Vessel Clip

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
SCHWARTZ VESSEL CLIP FDA UDI
Generic Name
Ligation clip, metallic FDA UDI
Device Name
SCHWARTZ VESSEL CLIP ANGLED FDA UDI
Model / Reference
2100-891 FDA UDI
Description
SCHWARTZ VESSEL CLIP ANGLED FDA UDI

Identifiers

Primary DI / UDI-DI
B09921008910 FDA UDI
FDA Product Code
DXC FDA UDI
GMDN Term
Ligation clip, metallic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4450 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 1 Inch FDA UDI

Schwartz Vessel Clip by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 79f47899-de26-4b7c-ac25-c2d6f31930ee 36 fields · synced Jun 1, 2026