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Cloward Cervical Retractor

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Cloward Cervical Retractor FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
Cloward Cervical Retractor With 5 Pairs of Blades 64 Millimeter Spread FDA UDI
Model / Reference
416-130 FDA UDI
Description
Cloward Cervical Retractor With 5 Pairs of Blades 64 Millimeter Spread FDA UDI

Identifiers

Catalog Number
416-130 FDA UDI
Primary DI / UDI-DI
00192896106710 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Self-retaining surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Self-retaining surgical retractor, reusable

Cloward Cervical Retractor by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6a722f1d-2d64-4ff1-92fa-6802dffe21ef 35 fields · synced Jun 8, 2026