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St Marks Hand Retractor

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
ST MARKS HAND RETRACTOR FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
ST MARKS HAND RETRACTOR WITH LIP AND FIBER OPTIC LIGHT CARRIER/UNIVERSAL CONNECTOR TAPERS TO 3.5 CM ANGLED TIP FDA UDI
Model / Reference
508-325L FDA UDI
Description
ST MARKS HAND RETRACTOR WITH LIP AND FIBER OPTIC LIGHT CARRIER/UNIVERSAL CONNECTOR TAPERS TO 3.5 CM ANGLED TIP FDA UDI

Identifiers

Catalog Number
508-325L FDA UDI
Primary DI / UDI-DI
00192896044401 FDA UDI
FDA Product Code
FDG FDA UDI
GMDN Term
Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4530 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

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

Category: Hand-held surgical retractor, reusable

St Marks Hand Retractor by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a11a1550-b139-4d7d-bf9f-79b20f712ac9 36 fields · synced May 31, 2026