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Edge Biologicals Inc

FDA UDI

Class I (US FDA UDI)

by Edge Biologicals, Inc.

Identity

Trade Name
EDGE BIOLOGICALS INC FDA UDI
Generic Name
Saline suspension medium/diluent IVD FDA UDI
Device Name
SALINE 0.45% 3ML FDA UDI
Model / Reference
T0601 FDA UDI
Description
SALINE 0.45% 3ML FDA UDI

Identifiers

Primary DI / UDI-DI
B645T0601 FDA UDI
FDA Product Code
JSC FDA UDI
GMDN Term
Saline suspension medium/diluent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2350 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Edge Biologicals Inc by Edge Biologicals, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e4c0340-5339-4d0e-9042-15738d6e4970 34 fields · synced Jun 8, 2026