← Back to catalogue

Universal Block Procedure Trays

FDA UDI

Class II (US FDA UDI)

by Distribution Unlimited, Llc

Identity

Trade Name
Universal Block Procedure Trays FDA UDI
Generic Name
General surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
include a wide selection of support materials and quality components needed to perform many pain management procedures. FDA UDI
Model / Reference
1 FDA UDI
Description
include a wide selection of support materials and quality components needed to perform many pain management procedures. FDA UDI

Identifiers

Catalog Number
DU3640 FDA UDI
Primary DI / UDI-DI
00850014433642 FDA UDI
FDA Product Code
OFQ FDA UDI
PUI FDA UDI
NAB FDA UDI
FPA FDA UDI
FMF FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5120 FDA UDI
878.4370 FDA UDI
878.4014 FDA UDI
880.5440 FDA UDI
880.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI
Total Volume — 5 Milliliter FDA UDI
Total Volume — 10 Milliliter FDA UDI
Needle Gauge — 25 Gauge FDA UDI
Shaft Length — 1.5 Inch FDA UDI
Needle Gauge — 18 Gauge FDA UDI

Category: General surgical procedure kit, non-medicated, single-useHypodermic needle, single-useIntravenous administration tubing extension setGeneral-purpose syringe, single-use

Universal Block Procedure Trays by Distribution Unlimited, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical dressing/drape kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f3cf6940-962a-4349-9202-589be4688602 35 fields · synced May 30, 2026