← Back to catalogue

Sterling Medical Products

FDA UDI

by Apollo Medical Products Corp.

Identity

Trade Name
Sterling Medical Products FDA UDI
Generic Name
Pellet implantation cannula, single-use FDA UDI
Device Name
TROCAR HORMONE Pellet Kit 32MM SS BETADINE MED GLOVE FDA UDI
Model / Reference
8109 FDA UDI
Description
TROCAR HORMONE Pellet Kit 32MM SS BETADINE MED GLOVE FDA UDI

Identifiers

Primary DI / UDI-DI
00685404002883 FDA UDI
GMDN Term
Pellet implantation cannula, single-use FDA UDI

Classification

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

Category: Pellet implantation cannula, single-use

Sterling Medical Products by Apollo Medical Products Corp. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pellet implantation cannula, 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 cdabca56-4945-4466-9bf0-4769a726d303 34 fields · synced May 30, 2026