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Caspar Lumbar Specula

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
CASPAR LUMBAR SPECULA FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
CASPAR LUMBAR SPECULUM NON-REFLECTIVE BLACK ANNODIZED COATED FDA UDI
Model / Reference
416-825 FDA UDI
Description
CASPAR LUMBAR SPECULUM NON-REFLECTIVE BLACK ANNODIZED COATED FDA UDI

Identifiers

Catalog Number
416-825 FDA UDI
Primary DI / UDI-DI
00192896079427 FDA UDI
FDA Product Code
FXE FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.1800 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

Dimensions & Sizes

Size
Width — 18 Millimeter FDA UDI
Length — 65 Millimeter FDA UDI

Category: Surgical retractor/retraction system blade, reusable

Caspar Lumbar Specula by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 81b1d21f-555d-4fde-a813-1e03f6362d76 36 fields · synced May 30, 2026