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Sontec Suture Ruler

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
SONTEC SUTURE RULER FDA UDI
Generic Name
Medical ruler, reusable FDA UDI
Device Name
HEARTLINE SONTEC SUTURE RULER FDA UDI
Model / Reference
2800-600 FDA UDI
Description
HEARTLINE SONTEC SUTURE RULER FDA UDI

Identifiers

Primary DI / UDI-DI
B09928006000 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Medical ruler, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 14.25 Inch FDA UDI

Sontec Suture Ruler by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd2c3d57-925c-4a0d-998e-7dd906f34a79 36 fields · synced May 31, 2026