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Msi

FDA UDI

Class I (US FDA UDI)

by Modern Surgical Instruments LLC

Identity

Trade Name
MSI FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Caspar Micro Lumbar Discectomy: 17-7500 Retractor Ball Snap Micro Lumbar Distractor, UDI 00810130201167 17-7410 Caspar Blade Lateral length 40mm to 43mm black titanium coated, UDI 00810130201297 17-7415 Caspar Blade Lateral length 45mm to 48mm black titanium coated, UDI 00810130201303 17-7420 Caspar Blade Lateral length 50mm to 53mm black titanium coated, UDI 00810130201310 17-7425 Caspar Blade Lateral length 55mm to 58mm black titanium coated, UDI 00810130201327 17-7430 Caspar Blade Lateral length 60mm to 63mm black titanium coated, UDI 00810130201334 17-7435 Caspar Blade Lateral length 65mm to 68mm black titanium coated, UDI 00810130201341 17-7440 Caspar Blade Lateral length 75mm to 78mm black titanium coated, UDI 00810130201358 17-7205 Caspar Specula 40mm length black, titanium coated surface, UDI 00810130205509 17-7210 Caspar Specula 45mm length black, titanium coated surface, UDI 00810130201174 17-7215 Caspar Specula 50mm length black, titanium coated surface, UDI 00810130205516 17-7220 Caspar Specula 55mm length black, titanium coated surface, UDI 00810130201181 17-7225 Caspar Specula 60mm length black, titanium coated surface, UDI 00810130205523 17-7230 Caspar Specula 65mm length black, titanium coated, UDI 00810130201198 17-7235 Caspar Specula 75mm length black, titanium coated surface, UDI 00810130201204 17-7512 Retractor Blade Ejector, UDI 00810130205530 29-6885 Tray for Caspar Specula: LD Tray with Lid, Dimensions: 537 x 250 x 100mm (L x W x D), incl. 2 inserts UDI 00810130201686 FDA UDI
Model / Reference
17-7200 FDA UDI
Description
Caspar Micro Lumbar Discectomy: 17-7500 Retractor Ball Snap Micro Lumbar Distractor, UDI 00810130201167 17-7410 Caspar Blade Lateral length 40mm to 43mm black titanium coated, UDI 00810130201297 17-7415 Caspar Blade Lateral length 45mm to 48mm black titanium coated, UDI 00810130201303 17-7420 Caspar Blade Lateral length 50mm to 53mm black titanium coated, UDI 00810130201310 17-7425 Caspar Blade Lateral length 55mm to 58mm black titanium coated, UDI 00810130201327 17-7430 Caspar Blade Lateral length 60mm to 63mm black titanium coated, UDI 00810130201334 17-7435 Caspar Blade Lateral length 65mm to 68mm black titanium coated, UDI 00810130201341 17-7440 Caspar Blade Lateral length 75mm to 78mm black titanium coated, UDI 00810130201358 17-7205 Caspar Specula 40mm length black, titanium coated surface, UDI 00810130205509 17-7210 Caspar Specula 45mm length black, titanium coated surface, UDI 00810130201174 17-7215 Caspar Specula 50mm length black, titanium coated surface, UDI 00810130205516 17-7220 Caspar Specula 55mm length black, titanium coated surface, UDI 00810130201181 17-7225 Caspar Specula 60mm length black, titanium coated surface, UDI 00810130205523 17-7230 Caspar Specula 65mm length black, titanium coated, UDI 00810130201198 17-7235 Caspar Specula 75mm length black, titanium coated surface, UDI 00810130201204 17-7512 Retractor Blade Ejector, UDI 00810130205530 29-6885 Tray for Caspar Specula: LD Tray with Lid, Dimensions: 537 x 250 x 100mm (L x W x D), incl. 2 inserts UDI 00810130201686 FDA UDI

Identifiers

Primary DI / UDI-DI
00810130205547 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Surgical retractor/retraction system blade, 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retractor/retraction system blade, reusable

Msi by Modern Surgical Instruments LLC — 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

Manufacturer
Modern Surgical Instruments LLC

Sources (1)

  • FDA UDI 0b23c79a-c1fa-4554-8a71-9ed5c871cd9d 33 fields · synced Jun 8, 2026